<?xml version="1.0" encoding="ISO-8859-1"?>
<oreganno>
<recordSet>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>22-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Reduced warfarin requirement population</comment>
<date>22-Sep-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>79001</geneId>
<geneName>VKORC1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>1</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15930419</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000002</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY HAPLOTYPE</type>
<variationSet>
<variation>
<date>22-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gcacagtggctcacgcctgtaatcccagcactttaggaagccaaggagggTggatcatgaggtcaggagtttgagaccagcctggccaatatggtgaaacc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gcacagtggctcacgcctgtaatcccagcactttaggaagccaaggagggCggatcatgaggtcaggagtttgagaccagcctggccaatatggtgaaacc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>22-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>atccctctgggaagtcaagcaagagaagacctgaaaaacaaccattggccGggtgcggtggctcacgcctataatcctagcattttgggaggccgaggtgg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>atccctctgggaagtcaagcaagagaagacctgaaaaacaaccattggccAggtgcggtggctcacgcctataatcctagcattttgggaggccgaggtgg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>22-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>catggaatcctgacgtggccaaaggtgcccggtgccaggagatcatcgacCcttggactaggatgggaggtcggggaacagaggatagcccaggtggcttc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>catggaatcctgacgtggccaaaggtgcccggtgccaggagatcatcgacTcttggactaggatgggaggtcggggaacagaggatagcccaggtggcttc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>22-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>atgcaatcttggtgatccacacagctgacagccagctagctgctcatcacGgagcgtcctgcgggtggggatgtggggaggtaactaacaggagtctttta</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>atgcaatcttggtgatccacacagctgacagccagctagctgctcatcacCgagcgtcctgcgggtggggatgtggggaggtaactaacaggagtctttta</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>22-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tcacccttcccagctccagagaaggcatcactgagggaggcccagcaccaCggtcctggctgacacatggttcagacttggccgatttatttaagaaattt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tcacccttcccagctccagagaaggcatcactgagggaggcccagcaccaTggtcctggctgacacatggttcagacttggccgatttatttaagaaattt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>23-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>High warfarin requirement group</comment>
<date>23-Sep-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>79001</geneId>
<geneName>VKORC1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15930419</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000001</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY HAPLOTYPE</type>
<variationSet>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gcacagtggctcacgcctgtaatcccagcactttaggaagccaaggagggTggatcatgaggtcaggagtttgagaccagcctggccaatatggtgaaacc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gcacagtggctcacgcctgtaatcccagcactttaggaagccaaggagggTggatcatgaggtcaggagtttgagaccagcctggccaatatggtgaaacc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>atccctctgggaagtcaagcaagagaagacctgaaaaacaaccattggccGggtgcggtggctcacgcctataatcctagcattttgggaggccgaggtgg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>atccctctgggaagtcaagcaagagaagacctgaaaaacaaccattggccGggtgcggtggctcacgcctataatcctagcattttgggaggccgaggtgg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>catggaatcctgacgtggccaaaggtgcccggtgccaggagatcatcgacCcttggactaggatgggaggtcggggaacagaggatagcccaggtggcttc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>catggaatcctgacgtggccaaaggtgcccggtgccaggagatcatcgacCcttggactaggatgggaggtcggggaacagaggatagcccaggtggcttc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>atgcaatcttggtgatccacacagctgacagccagctagctgctcatcacGgagcgtcctgcgggtggggatgtggggaggtaactaacaggagtctttta</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>atgcaatcttggtgatccacacagctgacagccagctagctgctcatcacGgagcgtcctgcgggtggggatgtggggaggtaactaacaggagtctttta</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tcacccttcccagctccagagaaggcatcactgagggaggcccagcaccaCggtcctggctgacacatggttcagacttggccgatttatttaagaaattt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tcacccttcccagctccagagaaggcatcactgagggaggcccagcaccaCggtcctggctgacacatggttcagacttggccgatttatttaagaaattt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>The CT60 polymorphism is 3' of the CTLA4 gene and is associated to Grave's Disease.  The allele was confirmed
						using ASTQ (allele-specific transcript quantification) to reduce expression.</comment>
<date>19-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>19-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>19-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00009</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00004</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1493</geneId>
<geneName>CTLA4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>3</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12724780</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000000</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>19-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ttttgatttcttcaccactatttgggatataacAtgggttaacacagacata</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs3087243</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ttttgatttcttcaccactatttgggatataacGtgggttaacacagacata</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>23-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Upregulated 2.9 fold (No change to steady-state expression using RT-PCR)</comment>
<date>23-Sep-2005</date>
<evidenceClassStableId>OREGEC00003</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00012</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00005</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>9628</geneId>
<geneName>RGS6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>4</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15375002</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000003</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ccaggccctggacctgcggtaggaaCggtcaggaggactgcatcaggcccg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2074647</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ccaggccctggacctgcggtaggaaTggtcaggaggactgcatcaggcccg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>23-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Unknown factor bound; Likely not AP2; Expression; T allele drives expression 2.8-fold; C allele drives expression 2.2-fold.</comment>
<date>23-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3938</geneId>
<geneName>LCT</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>5</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12915462</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000004</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gataagataatgtagCccctggcctcaaag</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs4988235</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gataagataatgtagTccctggcctcaaag</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>23-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Confirmed that differential binding occured for this polymorphism.  Binding occured for T allele.</comment>
<date>23-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Confirmed binding of C/EBP Beta to binding site.</comment>
<date>23-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3576</geneId>
<geneName>IL8</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>6</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15085176</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GTTGTTCAAT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000005</stableId>
<tfId>1051</tfId>
<tfName>CEBPB</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>23-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>aaagaactctaactctttatataggaagtTgttcaatgttgtcagtt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2227306</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>aaagaactctaactctttatataggaagtCgttcaatgttgtcagtt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Test population Ethiopian</comment>
<date>27-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>27-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Likely ETS-family binding site</comment>
<date>27-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>In the presence of TCDD enzyme this allele had altered expression activity.  However, without the TCDD, the results were inconclusive (for altered expression).</comment>
<date>27-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1544</geneId>
<geneName>CYP1A2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>11</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12920202</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>ACCCTGAACCCTAAAGACAGCTGTACCTTCATCCCCAGGGACCCAGCACCCCTTCTGGCCTATCCCCAAAGAGTCACCCTGGGTCTTAGGTAGTAGGTGGAGCTGAGGGATAATGGCCCAAGGCCAAGAGTTGATCCTTCCAACTTTGTTCAGTGATCCAGCTTTCATATCAGGTGATCAGGACAACCAGGCCAATCTGATAGGGGGCGGTGTTTATAAAAAGGCCACTCACCTAGAGCCAGAAGCTCCACACCAGCCATTACAACCCTGCCAATCTCAAGCACCTGCCTCTACAGGTACCTTTCTTGGGACCAATTTACAATCTCTGGGATCCCCAACTATAGAACCTGGAAGCTAGTGGGGACAGAAAGACGGGGAGCCTGGGCTAGGTGTAGGGGTCCTGAGTTCCGGGCTTTGCTACCCAGCTCTTGACTTCTGTTTCCCGATTTTAAATGAGCAGTTTGGACTAAGCCATTTTTAAGGAGAGCGATGGGGAGGGCTTCCCCCTTAGCACAAGGGCAGCCCTGGCCCTGGCTGAAGCCCAACCCCAACCTCCAAGACTGTGAGAGGATGGGGACTCATCCCTGGAGGAGGTGCCCCTCCTGGTATTGATAAAGAATGCCCTGGGGAGGGGGCATCACAGGCTATTTGAACCAGCCCTGGGACCTTGGCCACCTCAGTGTCACTGGGTAGGGGGAACTCCTGGTCCCTTGGGTATATGGAAGGTATCAGCAGAAAGCCAGCACTGGCAGGGACTCTTTGGTACAATACCCAGCATGCATGCTGTGCCAGGGGCTGACAAGGGTGCTGTCCTTGGCTTCCCCATTTTGGAGTGGTCACTTGCCTCTACTCCAGCCCCAGAAGTGGAAACTGAGATGATGTGTGGAGGAGAGAGCCAGCGTTCATGTTGGGAATCTTGAGGCTCCTTTCCAGCTCTCAGATTCTGTGATGCTCAAAGGGTGAGCTCTGTGGGCCCAGGACGCATGGTAGATGGAGCTTAGTCTTTCTGGTATCCAGCTGGGAGCCAAGCACAGAACACGCATCAGTGTTTATCAAATGACTGAGGAAATGAATGAATGAATGTCTCCATCTCAACCCTCAGCCTGGTCCCTCCTTTTTTCCCTGCAGTTGGTACAG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000008</stableId>
<tfId>UNKNOWN-ETS</tfId>
<tfName>UNKNOWN-ETS</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>27-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tgagttcCgggctttgctacccag</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs12720461</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tgagttcTgggctttgctacccag</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>The TATA binding protein (TBP) was demonstrated to be disrupted in the presence of the G allele resulting in 50% decreased expression from wild-type. </comment>
<date>28-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>28-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell type: human hepatoma cell line, B16A2</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1548</geneId>
<geneName>CYP2A6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>12</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>11394901</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000009</stableId>
<tfId>TBP</tfId>
<tfName>TBP</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>28-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>catccctctttttcaggcagtaTaaaggcaaaggagggg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>catccctctttttcaggcagtaGaaaggcaaaggagggg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>28-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>When allele (G) present, CYP2A6 is expressed at 48% of wild-type activity.</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>ROughly two to four-fold lower affinity for nuclear extracts in the presence of the variant (G) allele.</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1548</geneId>
<geneName>CYP2A6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>14</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14974084</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000012</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>28-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tgcccactgtctgttttctgtcctctgtAgatctttatataaaatgag</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs4803381</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tgcccactgtctgttttctgtcctctgtGgatctttatataaaatgag</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>28-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>The TATATAA sequence is important for the binding of a larger DNA-complex, but a smaller complex is able to bind the upstream part of this region (TTCTGTCCTCTGTAGATCTT)</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1548</geneId>
<geneName>CYP2A6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>15</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14974084</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>TTCTGTCCTCTGTAGATCTTTATATAA</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTCTGTCCTCTGTAGATCTTTATATAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>CTCACACATGTCCCCTGCCCACTGTCTGTTTTCTGTCCTCTGTAGATCTTTATATAAAATGAGAAACATAAACAACAATCATAATATTA</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000013</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>28-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>NF-Y pulled down search sequence.</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00005</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00003</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Competition eliminated with variant allele (G).</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: Human hepatoma HepG2.  22% reduction in activity with variant (G) allele.</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1548</geneId>
<geneName>CYP2A6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>19</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15247629</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GAGGATCTGGGTTGGAAACCAGCGGACAACCCTTGGGACACTTGAGATTTTTCCACCATTTGGGGGTTGTTATTACTATTTCTCCAGACCTAGCCAATCCCTCTGCCAACCGCTAACTCCAGGTACTCTTCTCCAGGTGTGGGGAAAGTTCCCCTGAAATATGGCTCTGGTCTTCCTCCCCTTCCCAATCAGAGATGGGCAGTGGAGGTTCTATGGCACCCATCCTGGCCTCACTCTGAGGTTCCAATGAGGATTCTGGGCATCAAGAGACAGCTCTGGGCAAAAGCAAAATCAAGTCAGCCCCTGGACCCAGTGCTGGGCTGCTGG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CCAAT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000019</stableId>
<tfId>4800</tfId>
<tfName>NFYA</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>28-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ctccccttcccaAtcagagatggg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ctccccttcccaGtcagagatggg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Neutral outcome entered.  Primary authors indicate that depth of population sampling cannot only supports a minor role of this haplotype in determing the ultrarapid metabolizer group.</comment>
<date>28-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>28-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Variant associated to ultrarapid metabolizer group.</comment>
<date>28-Sep-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1565</geneId>
<geneName>CYP2D6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>20</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>NEUTRAL OUTCOME</outcome>
<reference>11207030</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000020</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY HAPLOTYPE</type>
<variationSet>
<variation>
<date>28-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>caacttggaagaaccCggtctctacaaaaa</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>caacttggaagaaccGggtctctacaaaaa</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>29-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2 Human hepatocarcinoma</comment>
<date>29-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>22</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GGTACCTGGTTCATCTCATTGGGACTGGTTGGACAAGAGGGTGCAGCCCACGGAGGGTGAGCCAAAGCAGGGTGGGGCGTCGCCTCACCTGGGAAGCACAAGGGGTCGTGGAATTTTCTCCCCTACCCAAGGAAAGCCATAAGGGACTGAGCCTGAGGAACTGTGCACTCTGGCCCAGATACTGCACTTTTCCCATGGTCTTTGCAACCCGCAGACCAGGAGATTCCCTCCGGTGCCTATGCCACCAGGGCCCTGGGTTTCAAGCACAAAACTGGGCAGCCATTTGGGCAGACACCGAACTAGCTGCAGGAGTTTTTTTTTTTTTTTTTCCATACCCCATTGGCACCTGGAACGCCAGTGAGACAGAACCGTTCACTCCCCTGGAAAGGGGGCTGAAACCAGGGATCCAAGTGGTCTGGCTCGGTGGGCCCCACCCCCATGGAGCCCAGCAAACAAAGATTCACTTGGCTTGAAATTCTTGCTGCCAGCACAGCAGCAGTCTGAGATTGACCTGGGACCCTCGAACTTGGTTGGGTGCTGTGGGGGGGCATCTTCCATTGCTGAGGCTTGAGTAGGTGGTTTTACCTTCGCGGTGTAAACAAAGCTGCTGGGAAGTTTGAACTGGGTGGAGCTCACCACAGCTCAGTAAGGCCACTGTGGCCAGACTGCCTCTCTGGATTTCTCCTCTCTGGGAAGGATATCTCTGAAAAAAAGGCAGCAGCCCCAGTCAGGGACTTATAGATGAAACCCCCATCTCCCTGGGACAGAGCCCCTCGGGGAAGAGGTGGCTTCCACCATTGTGGAAGACTGTGTGGCAATTCCTCACGGATTTAGAACTAGAGATACCATTTGACCCAGCAATCCCATTACTGGGTGTATACCCATAGGATTATAAATCATTCTACTATAAAGACACATGCACACTTATGTTTATTGTAACACTATTTACAATAGCAATGACCTGGAACCAATCCAAAAGCCCATCAATGATAGACTGAATAAAGAAAATGTGGCACATATACACTGTGGAATACTATGCAGCCATAAAAAAGGATGAGTTCATGTCCTTTGCAGAGACATGGATGAAGCTGGAAACCATCATTCTCAGCAAACTAGCACAATAACAGAAAACCAAACACTGCATGTTGTCACTCATAAGTGGGAGTTAAACAATGAGAACACATGGACACAGGGAGGGGAACGTCACACACTGGGGCATGTCGGGGAGTGGGGGCCTACGGGAGGGATAGCATTAGCAGAAATACCTAATGTAGGTGACGGGTTGATGGGTGCAGCAAACCACCATGGCACATATACACCTATGTAATAAAACTGCACGTTCTGCACATGTACCCCAGAACTTAAAGTATAATTAATAATAATAATAATTTCTGGGCATGTAAGTAGCTGTCTTTCAGGTTCTACTTTGATACATATTCTGAGAGAATTAAACCTGTCAAAGAAACCTTGACTTTCAATGGCAGGCACTGGAATTGACCCTAATAATGTGTTTTGGGGTAAGCCTACTCATATTCTCAACCTGTCTGCAGTAGTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCTTCCGTAGGTCACTCTGTGGCTCAGAGACCCTGCTTAGCAAGCGCCCAACCTTTCAATTATTTGTTCAGTAAAACTTGAACTCATGTCTCCCCTTCTTGATAAAAAGAAAATACGTTATGTAATGTCGGGTTACTCTATAACTCTTGTCCTGTCTCTCGGCAACTACTGAACTAACTGTTTTCATATTGAGCAAACGTTTATGGAAGGACTGCCAAGAGTCAGGTACTAGGCTTGGTAATATTCCCCGTTCTCTCTAGTCAAAGCCAACACCAGCCAGACTTGCAGATCTAGGTCCCAAGCCCACTGCAGATCACAGGCCAGGGTCTGGTCTCCTCTGAGCTCCTTTGGGAGGGAAAGACAGAATTATTAACACCCATTTTGTAGATTAGGCAACTGAGGCTGAGGAAGTTTAAATAACTCAGACAGGGCCTGCACGTCAGTCATATTCCAA</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CCTGTCTGCAGTAGTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCTTCCGTAGGTCACTCTGTGGCTCAGAGACCCTGCTTAGCAAGCGCCCAACCTTTCAATTATTTGTTCAGTAAAACTTGAACTCATGTCTCCCCTTCTTGATAAAAAGAAAATACGTTATGTAATGTCGGGTTACTCTATAACTCTTGTCCTGTCTCTCGGCAACTACTGAACTAACTGTTTTCATATTGAGCAAACGTTTATGGAAGGACTGCCAAGAGTCAGGTACTAGGCTTGGTAATATTCCCCGTTCTCTCTAGTCAAAGCCAACACCAGCCAGACTTGCAGATCTAGGTCCCAAGCCCACTGCAGATCACAGGCCAGGGTCTGGTCTCCTCTGAGCTCCTTTGGGAGGGAAAGACAGAATTATTAACACCCATTTTGTAGATTAGGCAACTGAGGCTGAGGAAGTTTAAATAACTCAGACAGGGCCTGCACGTCAGTCATATTCCAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000022</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Enhancer activity reduced by 64% in presence of allele (TGT).   Allele is rare in French population.  Cell line is human liver.</comment>
<date>29-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>29-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: Human liver HepG2</comment>
<date>29-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment></comment>
<date>29-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>23</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CATGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000023</stableId>
<tfId>7391</tfId>
<tfName>USF1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>29-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gcatcaagaacatgtggttctaatgg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gcatcaagaacatgtTGTggttctaatgg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Binding sequence was determined computationally as the canonical binding sequence.  Only the 3' most AA sequence of the binding site was biologically tested.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Antibodies to HNF-4alpha not HNF-4gamma supershifted bound complex.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>aagttcatgtgcaCCgttgagttaatt (AA to CC mutation in HNF-4 binding site as competitor) does not compete for binding with HNF-4 sequence.  HNF-4 sequence in excess competes out complex formation.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>aagttcatgtgcaCCgttgagttaatt (AA to CC mutation in HNF-4 binding site) reduces enhancer activity by 19%</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>54</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TCATGTGCAAAGTTGAGTT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>GTAGTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACA</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000053</stableId>
<tfId>3172</tfId>
<tfName>HNF4A</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Binding sequence was determined computationally as the canonical binding sequence. Only the CTT sequence of the binding site was biologically tested.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Antibodies to HNF-4alpha supershifted bound complex.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>ggaagctttgaaAGCagctcatagaa (CTT to AGC mutation in HNF-4 binding site as competitor) does not compete for binding with HNF-4 sequence. HNF-4 sequence in excess competes out complex formation.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>ggaagctttgaaAGCagctcatagaa (CTT to AGC mutation in HNF-4 binding site) reduces enhancer activity by 44%</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>55</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CTTTGAACTTAGCTCATAG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>GTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAG</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000054</stableId>
<tfId>3172</tfId>
<tfName>HNF4A</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Binding sequence was determined computationally as the canonical binding sequence. Only the AAC sequence of the binding site was biologically tested.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Antibodies to HNF-1 supershifted bound complex.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>ttaattgtttaatattcCTGaagga (AAC to CTG mutation in HNF-1 binding site as competitor) does not compete for binding with HNF-1 sequence. HNF-1 sequence in excess competes out complex formation.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>ttaattgtttaatattcCTGaagga (AAC to CTG mutation in HNF-1 binding site) reduces enhancer activity by 30%</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>56</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTGTTTAATATTCAACA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>ATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGA</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000055</stableId>
<tfId>6927</tfId>
<tfName>TCF1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Binding sequence was determined computationally as the canonical binding sequence. Only the GTG sequence of the binding site was biologically tested.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Antibodies to USF1 supershifted bound complex.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>gcatcaagaacatTAGgttctaatgg (GTG to TAG mutation in E-box binding site as competitor) does not compete for binding with E-box sequence. E-box sequence in excess competes out complex formation.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>gcatcaagaacatTAGgttctaatgg (GTG to TAG mutation in E-box binding site) reduces enhancer activity 33%</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>57</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CATGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>GCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGA</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000056</stableId>
<tfId>7391</tfId>
<tfName>USF1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Binding sequence was determined computationally as the canonical binding sequence. Only the CGT sequence of the binding site was biologically tested.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Antibodies to USF1 supershifted bound complex.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>tgcccacggtcaTAAgagtaaacaac (CGT to TAA mutation in E-box binding site as competitor) does not compete for binding with E-box sequence. E-box sequence in excess competes out complex formation.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>tgcccacggtcaTAAgagtaaacaac (CGT to TAA mutation in E-box binding site) reduces enhancer activity by 43%</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>58</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CACGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>GAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGT</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000057</stableId>
<tfId>7391</tfId>
<tfName>USF1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Binding sequence was determined computationally as the canonical binding sequence. Mutation analysis of GT in binding site did not compete out binding in gel shift competition.  This is likely because the change from the canonical TG sequence wasn't significant enough (when compared to other binding sites from this reference).  However, this conclusion, is in disagreement with the effect observed in the reported gene assay in vitro (where the mutation caused a reduction in activity of 47%)</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Antibodies to USF1 supershifted bound complex.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>tcctcctaatcacaGTtctggtctga (mutation in E-box binding site of TG to GT) did not compete out binding.  However, binding was compete out in the presence of excess unlabelled E-box sequence.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>tcctcctaatcacaGTtctggtctga (mutation in E-box binding site of TG to GT) reduces enhancer activity by 47%</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>59</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CACATG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>TTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCC</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000058</stableId>
<tfId>7391</tfId>
<tfName>USF1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Binding sequence was determined computationally as the canonical binding sequence. Only the AC sequence of the binding site was biologically tested.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Addition of unlabelled CRE sequence in excess eliminated protein binding.  When competed with mutant CRE sequence, the binding was not abolished tgGAttca (change from AC to GA)</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Antibodies to Jun family super shifted complex.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>tgGAttca (change from AC to GA) mutation reduced enhancer activity by 80%</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>60</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14742674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GTCGTTAGAATCTGAACTTCCTGAAGTTCATGTGCAAAGTTGAGTTAATTGTTTAATATTCAACAAGGATTATGCCAGTAAGATGGTAGGAAAATATTAGATATGTGTCATCACTGCTGGTATTATTTAAACTGCAACATATTTTAGCTGGCTGCTGATCTCAGCCACCATGCCTGCATTTTATCTCTGTCTCGTGGTCTGCAACCTTGGAAGCTTTGAACTTAGCTCATAGAATCCTGGGCATCAAGAACATGTGGTTCTAATGGCTAGATAGGGAATGAGAGTAAAAGGATTTTGCCCACGGTCACGTGAGTAAACAACAGATTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGTCCTTTCATTTCCTCCTAATCACATGTCTGGTCTGATCTGGCTGTTTCCCACCTTCCAATTCCTGCCTTCTCCAATGCTCCCT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGACTTCA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>TTTGGAGGGGTCTGGACTACTGTGATGACTTCATTCTGACAATATGTTCCAGTTGT</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000059</stableId>
<tfId>AP1 (Jun family) CRE</tfId>
<tfName>AP1 (Jun family) CRE</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000092969</geneId>
<geneName>TGF-beta 2 (transforming growth factor b</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>61</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15647279</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AGTTCAGATCCGCCACTCCGCACCCGAGACTGACACACTGAACTCCAC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000060</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000092969</geneId>
<geneName>TGF-beta 2 (transforming growth factor b</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>62</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15647279</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CAAGCAGGATACGTTTTTCTGTTGGGCATTGACTAGATTGTTTGCAAAAG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000061</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000092969</geneId>
<geneName>TGF-beta 2 (transforming growth factor b</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>63</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15647279</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ATTTTTTTCTTCTTACTCGCCAAAGTCAGGGTTC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000062</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000092969</geneId>
<geneName>TGF-beta 2 (transforming growth factor b</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>64</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15647279</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AATATTTCCACTTTTGGAACTACTGGCCTTTTCTTTTTAAAGGAATT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000063</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000023287</geneId>
<geneName>RB1</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>65</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15618023</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GGCGGAAGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>ttccccacagacgccggcgggcccgggagcctcgcggacgtgacgccgcgGGCGGAAGTgacgttttcccgcggttggacgcggcgctcagttgccgggcg</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000064</stableId>
<tfId>E4TF1, Fli-1 (RBF Motif)</tfId>
<tfName>E4TF1, Fli-1 (RBF Motif)</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000023287</geneId>
<geneName>RB1</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>66</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15618023</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CGGGCGG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>agttccccacagacgccggcgggcccgggagcctcgcggacgtgacgccgCGGGCGGaagtgacgttttcccgcggttggacgcggcgctcagttgccggg</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000065</stableId>
<tfId>ENSG00000185591</tfId>
<tfName>Sp1</tfName>
<tfSource>ENSEMBL</tfSource>
<tfVersion>homo_sapiens_core_32_35a</tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000023287</geneId>
<geneName>RB1</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>67</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15618023</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CGGGCGGGGGA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>ccgcgggcggaagtgacgttttcccgcggttggacgcggcgctcagttgcCGGGCGGGGGAgggcgcgtccggtttttctcaggggacgttgaaattattt</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000066</stableId>
<tfId>ENSG00000185591</tfId>
<tfName>Sp1</tfName>
<tfSource>ENSEMBL</tfSource>
<tfVersion>homo_sapiens_core_32_35a</tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000023287</geneId>
<geneName>RB1</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>68</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15618023</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GGAAGTGACG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>cccacagacgccggcgggcccgggagcctcgcggacgtgacgccgcgggcGGAAGTGACGttttcccgcggttggacgcggcgctcagttgccgggcgggg</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000067</stableId>
<tfId>ENSG00000141510</tfId>
<tfName>p53(TP53)</tfName>
<tfSource>ENSEMBL</tfSource>
<tfVersion>homo_sapiens_core_32_35a</tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000023287</geneId>
<geneName>RB1</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>69</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15618023</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GTGACGTTT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>cagacgccggcgggcccgggagcctcgcggacgtgacgccgcgggcggaaGTGACGTTTtcccgcggttggacgcggcgctcagttgccgggcgggggagg</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000068</stableId>
<tfId>ENSG00000115966</tfId>
<tfName>ATF-2</tfName>
<tfSource>ENSEMBL</tfSource>
<tfVersion>homo_sapiens_core_32_35a</tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000023287</geneId>
<geneName>RB1</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>70</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15618023</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTTCCCGC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>cggcgggcccgggagcctcgcggacgtgacgccgcgggcggaagtgacgtTTTCCCGCggttggacgcggcgctcagttgccgggcgggggagggcgcgtc</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000069</stableId>
<tfId>ENSG00000101412</tfId>
<tfName>E2F-1 (E2F1)</tfName>
<tfSource>ENSEMBL</tfSource>
<tfVersion>homo_sapiens_core_32_35a</tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>16-Aug-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>16-Aug-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00000</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00000</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>ENSG00000023287</geneId>
<geneName>RB1</geneName>
<geneSource>ENSEMBL</geneSource>
<geneVersion>homo_sapiens_core_32_35a</geneVersion>
<id>71</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15618023</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AGAGGACGGGGCGTGCCCCGACGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>tccggtttttctcaggggacgttgaaattatttttgtaacgggagtcgggAGAGGACGGGGCGTGCCCCGACGTGcgcgcgcgtcgtcctccccggcgctc</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000070</stableId>
<tfId>ENSG00000141510</tfId>
<tfName>p53(TP53)</tfName>
<tfSource>ENSEMBL</tfSource>
<tfVersion>homo_sapiens_core_32_35a</tfVersion>
<type>TRANSCRIPTION FACTOR BINDING SITE</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Designated a low-penetrance allele by authors.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>The annotated variant allele has lower protein binding affinity (A allele).</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell-lines: MCF-7 and HepG2.  In MCF-7, 1.9 fold higher expression for reference allele (G allele).  In HepG2, this is 1.4 fold higher. (From 1999 study by same author)</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>72</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14673875</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000071</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>30-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>agacaagggcaGgagagaggc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2740574</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>agacaagggcaAgagagaggc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>The mutation is present in the canonical genome sequence it is A(T)10AT. </comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
<comment>
<comment>Record represents a deletion.  The variant sequence is present in hg18, while  the reference sequence with a deletion represents that changed sequence.</comment>
<date>26-Apr-2007</date>
<userName>bcb</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Allele frequence in 87 Japanese (60%), 50 Caucasion (39%), and African-American (44%).  The mutation is present in the canonical genome sequence it is A(T)10AT.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00011</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2 (human hepatoblastoma). Variant allele A(T)10AT has 2.6-fold more activity than reference A(T)9AT allele.  </comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>54600</geneId>
<geneName>UGT1A9</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>73</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15115919</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>CTCATATATTCTTGTTCTTTTGGGTAAATCATTGTCAGTGACTGATTTTTTTTTTATGAAAGGATAAAAACACGCCCTCTATTGGGGTCAGGTTTTGTGCTGGTATTTCTCCCACCTACTGTATCATAGGAGCTTAGATTCCCAGCTGCTTGCTCTCAGCTGCAGTTCTCTG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000072</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>30-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tcattgtcagtgactgatttttttttatgaaaggataa</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs3832043</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tcattgtcagtgactgatttttttttTatgaaaggataa</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>EMSA test was also performed but the annotated polymorphism did not alter binding of nuclear factors. </comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>In MC and C2C12 cell lines, activity with G allele was 1.4-fold higher than activity with C allele.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>2673</geneId>
<geneName>GFPT1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>74</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>NEUTRAL OUTCOME</outcome>
<reference>15878746</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000073</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>30-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>cttaatcatataaCcagccatagaa</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>cttaatcatataaGcagccatagaa</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Retested in 93 samples for serum resistin levels.  G/G genotype had higher serum resistin levels than C/C.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Nuclear proteins bound to the G allele but not to the C allele.  A competitor to G when added in excess competed out binding.  Cell line: 3T3-L1 adipocytes.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Identified polymorphism by resequencing ~1kb upstream of 24 Japanese patients with T2DM (Type 2 Diabetes Mellitus).</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Antibodies to Sp1 weakly affected protein binding.  Antibodies to Sp3 strongly affected protein binding.  Together, the complex was entirely supershifted.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment><![CDATA[
Cell line: Drosophila Schneider Line 2 (cell line lacks endogenous Sp family transcription factors).  When effctors (overexpressed Sp1), G allele significantly enhanced (> 3-fold).]]>
</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>56729</geneId>
<geneName>RETN</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>76</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15338456</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000075</stableId>
<tfId>Sp1 / Sp3</tfId>
<tfName>Sp1 / Sp3</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>30-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ccttcccacttccaacagggcctccGtcttcatgtccagagactggtcagg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs1862513</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ccttcccacttccaacagggcctccCtcttcatgtccagagactggtcagg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>The binding activity was constitutive as EMSA signal intensities not affected by clobetasol propionate or Terbutalin.  AP-2 was tested in complex but was not the causal transcription factor for differential expression.</comment>
<date>30-Sep-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>30-Sep-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>17-18% reduction in transcription from the C allele as compared to the T allele</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00009</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00004</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>One of the complexes shifted with the T allele was less abundant than a complex shifted with the C allele.</comment>
<date>30-Sep-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>154</geneId>
<geneName>ADRB2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>77</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15578262</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000076</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>30-Sep-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ccgcccgggccagccCcaggagaaggaggg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs11959427</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ccgcccgggccagccTcaggagaaggaggg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Search space sequence is the targetted EMSA sequence.</comment>
<date>1-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>1-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines: MDA-MB-231, MCF-7, HEK-293, and SL-2.  SL-2 line is Sp-1 deficient; demonstrated ~100-fold induction when contransfected with Sp1; EGFR expression dependent on Sp1.  Lower promoter activity observed with G allele compared to T allele.</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: MDA-MB-231.  Affinity of nuclear proteins to T allele was higher than G allele.  Assay with pure Sp1 demonstrated similar results.</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell type: Human fibroblast cells.  EGFR mRNA (using 10 cell lines with diplotype G-C/T-C) was ~40% higher with T allele than G allele.  (In vivo assay)</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00009</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00004</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1956</geneId>
<geneName>EGFR</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>78</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15665278</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>gcagcctccgccccccgcacggtgt</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>cctccgcccc</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000087</stableId>
<tfId>6667</tfId>
<tfName>SP1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>1-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ccgcagcagcctccGccccccgcacg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs712829</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ccgcagcagcctccTccccccgcacg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>1-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Protein bound with higher affinity to T allele than G allele and was competed out with excess unlabelled T-probe.</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Pre-incubation with antibody to Sp1 removed formation of complex.</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: Human myeloid leukaemia premonocyte cell line: THP-1.  Comparison of promoter activity show greater activity with T allele than G allele (D compared with F haplotype in reference)</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6696</geneId>
<geneName>SPP1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>79</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>16009426</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>CATCTAGAATAAATTACCATTCTTCTATTTCATATAGAATTTTATATTTTAATGTCACTAGTGCCATTTGTCTAAGTAACAAGCTACTGCATACTCGAAATCACAAAGCTAAGCTTGAGTAGTAAAGGACAGAGGCAAGTTTTCTGAACTCCTTGCAGGCTTGAACAATAGCCTTCTGGCTCTTCAATAAGTACAATCATACAGGCAAGAGTGGTTGCAGATATTACCTTTATGTTACTTAAACCGAAAGAAACAAAAATCCATTCTATTTAATTTTACATTAATGTTTTTCCCTACTTTCTCCCTTTTTCATGGGATCCCTAAGTGCTCTTCCTGGATGCTGAATGCCCATCCCGTAAATGAAAAAGCTAGTTAATGATATTGTACATAAGTAATGTTTTAACTGTAGATTGTGTGTGTGCGTTTTTGTTTTTTTTTGTTTTAACCACAAAACCAGAGGGGGAAGTGTGGGAGCAGGTGGGCTGGGCAGTGGCAGAAAACCTCATGACACAATCTCTCCGCCTCCCTGTGTTGGTGGAGGATGTCTGCAGCAGCATTTAAATTCTGGGAGGGCTTGGTTGTCAGCAGCAGCAGGAGGAGGCAGAGCACAGCATCGTCGGGACCAGACTCGTCTCAGGCCAGTTGCAGCCTTCTCAGCCAAACGCCGACCAAGGTACAGCTTCAGTTTGCTACTGGGTTGTGCAT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000088</stableId>
<tfId>6667</tfId>
<tfName>SP1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>1-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>atgacacaatctcTccgcctccctgtg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>atgacacaatctcGccgcctccctgtg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Association studies performed.</comment>
<date>1-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>1-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: COS-1 cells.  A allele demonstrated two-fold decrease in promoter activity compared to C allele.  </comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Mutant allele (A) showed little or no binding to (mouse) liver nuclear proteins and separately, weakly bound purified TFIID.  C allele showed binding of both liver nuclear proteins and purified TFIID (separately)</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>350</geneId>
<geneName>APOH</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>80</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12605674</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>CCAAGACATATTAAGAATGGATGAGGAGGACTTTGTATTGATCTGACGTAAGAGAAGATAGAGAATTCAAGGATAGCTCTAAGGTCCTAACTGGAGCTATAGGAGCTTGCAAGAGAGGATGTTGAGCTCAGTTTGTAGGGAATTAAAGTTGTAAGTGCCTCCTGGAAGACATTCTTTGTAATTATACATCTGAAAACTGGAACATCATTTTAGAGAGGTGGAGACTGAGAACAGAGAGTAGGTGTTTGTCCAAAGTTTATATGCCAAGGCTGTGAGTGAAACAGGAGCTTCGATCTTTTGGTGTTCCATCTACAACATACACAAAACAAAAGATGGAGAATGAGAAGTCCAGGCAACCCCGGAAACAACAAGTTTCTGTCAAAAGCAATAATGAACTGTTTTGTGCCATTAACAAAAACGTTATGAAGACAGAAACCATCTCCCAAAGATTTCATAACAGAGCCACATAAGTGGAAAGTAAATGATTAAAGAATGTGGGTCTCAGAGTTCCATTCAAATCATGATACTTTATCTTCTATTTACAAAGATAAAAGTACACCAGAAAATGGTTAATGTTTAAGCGCTTTCATATTTGGCTCTGTCTTTTTAGCAGACGAAAACCACTTTGGTAGTGCCAGTGTGACTCATCCACAATGATTTCTCCAGTGCTCATCTTGTTCTCGAGTTTTCTCTGCC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000089</stableId>
<tfId>TFIID</tfId>
<tfName>TFIID</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>1-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ctgtctttttagcagacgaaaacCactttggtagtgccagtgt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs8178822</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ctgtctttttagcagacgaaaacAactttggtagtgccagtgt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Polymorphism identified to increase transcription of CD14 by lowering the affinity of the CD14 regulatory region for Sp3 (inhibitory factor).</comment>
<date>1-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>1-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: Mono Mac 6 cells.  C allele had strong basal transcription activity.  T allele resulted in 32% increase in gene expression</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Tested Sp and AP2 oligonucleotides.  Sp family oligonucleotides competed out binding.  Similar results with HeLa nuclear extracts (competed out by Sp family oligonucleotides).  Mutation tests showed polymorphism affected affinity for Sp family binding.</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Tested with antibodies to Sp1, Sp2, and Sp3 successfully.</comment>
<date>1-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>929</geneId>
<geneName>CD14</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>81</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>11698458</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GGCGCCTGAGTCATCAGGACACTGCCAGGAGACACAGAACCCTAGATGCCCTGCAGAATCCTTCCTGTTACGGTCCCCCTCCCTGAAACATCCTTCATTGCAATATTTCCAGGAAAGGAAGGGGGCTGGCTCGGAGGAAGAGAGGTGGGGAGGTGATCAGGGTTCACAGAGGAGGGAACTGAATGACATCCCAGGATTACATAAACTGTCAGAGGCAGCCGAAGAGTTCACAAGTGTGAAGCCTGGAAGCCGGCGGGTGCCGCTGTGTAGGAAAGAAGCTAAAGCACTTCCAGAGCCTGTCCGG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000090</stableId>
<tfId>Sp1 / Sp2 / Sp3 (Sp family)</tfId>
<tfName>Sp1 / Sp2 / Sp3 (Sp family)</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>1-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>cttcctgttacggTccccctccctgaaacatc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2569190</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>cttcctgttacggCccccctccctgaaacatc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>2-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Leptin serum levels 50% higher than in AA than GA/GG genotypes.  Two-fold increase in adipose tissue leptin secretion by AA vs GA/GG subjects.  Population: 39 healthy female swedish subjects (10 GG, 18 GA, 11 AA)</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: U937 and subcutaneous adipocytes.  Nuclear factors bound with higher affinity to A allele.  Probe used is annotated as search space sequence.  One protein complex formed in U937 cells as opposed to two in human adipose tissue.   </comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3952</geneId>
<geneName>LEP</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>82</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12189581</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GCGACAGGGTTGCGCTGATCCTCC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000091</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>2-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tattcttcttttgttttgttttgcgacagggttgcGctgatcctcccgcctc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs7799039</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tattcttcttttgttttgttttgcgacagggttgcActgatcctcccgcctc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Flow cytometry showed a higher expression of human alpha-chain on plasmid carrying T allele.  </comment>
<date>2-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>2-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: PT18, and RBL-2H3.  Luciferase activity higher from T allele than C allele (construct annotated as search space sequence).  Similar results observed in KU812 cell line.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Performed with overproduced GATA-1.  T allele activity was ~4-fold higher than C allele (increased only 2-fold from previous assay).  T allele responded better to GATA-1.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Tested specific binding for GATA-1.  GATA-1 bound T allele at lower potential than canonical binding sequence.  Had two times greater affinity than C allele for GATA-1.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Resequenced 54 Japanese individuals.  96.2% of patients with atopic dermititis had T/T/ genotype</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>2205</geneId>
<geneName>FCER1A</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>83</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12902495</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GCTAGCCATGCTCCTGAATATGTATAAACAGTACATCATATGACTAAGAGTTTGACTTAGGGGTTAGATTTTATGTGTTTGAACCCCAAATTAGTTATTTAATAGTTGGCACCCCAAAACAAGTTACTTAACCTCACTAAGATTCAGTTTTCCTGTTTATAAAATGTAGATAGTGATAGTATGTACTTTATAGGATTATTGTGAAAAATAAATGAAATATCAGATTTATTTAGGATAACACCTGGCATATGTTTGGTATTCAGTAATTAGTTGCTGCTGTTTTATTCTGCTCTCCCTTGCATCCCACTTTTCTAAGTTGTAAACTAAATAGTTGTACACAGATTGACAGATTAAGAAAGGCTTGTGATTGTGCTAGACCTATGCCTCTCTCTCACCAGATTCCAGGTGTATATGTGGAGGTGGGATAGGGAGTGGAGTAAGTGGGTAAATATTAAATTGCCCAGTTGGGCACCATCCTGAATATTATCTCTAAAGAAAGAAGCAAAACCAGGCACAGCTGATGGGTTAACCAGATATGATACAGAAAACATTTCCTTCTGCTTTTTGGTTTTAAGCCTATATTTGAAGCCTTAGATCTCTCCAGCACAGTAAGCACCAGGAGTCCATGAAGAAGA</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000092</stableId>
<tfId>2623</tfId>
<tfName>GATA1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>2-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>agctgatgggttaaccagatatgaTacagaaaacattt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2251746</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>agctgatgggttaaccagatatgaCacagaaaacattt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Authors noted variant causes new CCAAT box in mutant sequence.  Mutation detected from 2 Chinese Type 2 diabetes mellitus patients.</comment>
<date>2-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>2-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>HeLa cells transfected.  C allele had higher activity (15.7% +/- 4.1%) than A allele (5.7% +/- 2.9%).  Used B-Gal assay.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>T had slower shift mobility that WT C allele.  Authors suggested role as possible repressor.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>231</geneId>
<geneName>AKR1B1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>84</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>14515207</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>CGCTAAAGCATTCGCTTTCCCACCAGATACAGCAGCTGAGGAACTCCTTTCTGCCACGCGGGGCGCGGGCGAGCGTTGGGGGCGGAAAGAATCCGCTGCCACTAGGACCAGGCGGAAGAAGCATCCCCGCCGACCCTTGGGGAAGGCCGCCGCGGCACCCCCAGCGCAACCAATCAGAAGGCTCCTTCGCGCAGCGGCGCGCCAACCGCAGGCGCCCTTTCTGCCGACCTCACGGGCTATTTAAAGGTACGCGCCGCGGCCAAGGCCGCACCGTACTGGGCGGGGGTCTGGGGAGCGCAGCAGCCAT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000093</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>2-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>cggaaagaatccgctgccaCtaggaccaggcggaaga</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>cggaaagaatccgctgccaAtaggaccaggcggaaga</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>2-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines: Calu-3, CF-PAC1, and HeLa.  A allele had increased promoter activity  by 60%, 66%, and 45% in the respective cell types.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Oligonucleotides assayed harboring various cis-acting consensus sequences.  Minimal promoter may act with SRF-like protein.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Tested SRF-1 and YY1 protein.  Factors could both occupy variant binding region.</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Supershift against transcription factors binding YY1 and CArG sites.  Supershifted YY1 not SRF1</comment>
<date>2-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1080</geneId>
<geneName>CFTR</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>85</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>10652351</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GGCTGGGAGTCAGAATCGGGAAAGGGAGGTGCGGGGCGGCGAGGGAGCGAAGGAGGAGAGGAGGAAGGAGCGGGAGGGGTGCTGGCGGGGGTGCGTAGTGGGTGGAGAAAGCCGCTAGAGCAAATTTGGGGCCGGACCAGGCAGCACTCGGCTTTTAACCTGGGCAGTGAAGGCGGGGGAAAGAGCAAAAGGAAGGGGTGGTGTGCGGAGTAGGGGTGGGTGGGGGGAATTGGAAGCAAATGACATCACAGCAGGTCAGAGAAAAAGGGTTGAGCGGCAGGCACCCAGAGTAGTAGGTCTTTGGCATTAGGAGCTTGAGCCCAGACGGCCCTAGCAGGGACCCCAGCGCCCGAGAGACCATGC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000094</stableId>
<tfId>7528</tfId>
<tfName>YY1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>2-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gaaagccgctagagcaaatTtggggccggaccaggcagc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gaaagccgctagagcaaatAtggggccggaccaggcagc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>3-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: MIN6.  A allele showed a doubling of IAPP promoter activity compared to G allele.  Effect demonstrated on basal transcription.</comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>No binding in G allele.  Binding detected in A allele.</comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Tested CRE, TTF-2, AP-1, GRE, and HNF3 oligonucleotides.  Competition detected with CRE.  Slight competition detected with TTF-2.</comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>anti-CREB, anti-CREM, and anti-CBP tested.  Supershifted with anti-CREB.  CREB peptide addition abolished complex.</comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3375</geneId>
<geneName>IAPP</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>86</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15243700</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>ACTTCTGCTGTGTATGACACACCATTAACTGCACAAGGACACTGTGTATTTGCTACGTTAATATTTACTGATGAGTTAATGTAATAATGACCCATCCGCTTCTGCTGCCTGTGAGGTACTTTCTATCTATAGGGATGGAAATTAATGACAGAGGCTCTCTGAGCTGCCTGATGTCAGAGCTGAGAAAGGTGTGAGGGGTATATAAGAGCTGGATTACTAGTTAGCAAATGAGGGGGTAAATATTCCAGTGGATACAAGCTTGGACTCTTTTCTTGAAGCTTTCTTTCTATCAGAAGCATTTGCTGATATTGCTGACATTGAAACATTAAAAGGTAAAGAATTTCCTATTTCTGGGAAAGTTTTATTTATTTAGAGAAATGCACACTTGGTGTTAAATTCATGGTTTATTTCAAAGAAAGGCTAAAGGGAGAATGTATTACAATATAAATGTTCAGATTGCTTAGAGAAGGAAATTGGGAAAGTAAAAATCTCGAAATTACTTGAAAAGTGGACAATATTAAGGGACTGTATCAATAAAAATTTTGATCCTTGTAAATTACGTTTTAAAAAGATGTTTCTTTTAAAAACTAAGCTCTAATTTAAAATTACATCAATTAGAACTGTAAGAAATCTCTTGATTTCAGTGCTGGATTATTCTTTGCAGAAAATTTGAGAAGCAATGGGCATCC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000095</stableId>
<tfId>1385</tfId>
<tfName>CREB1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>3-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tgacccatccGcttctgctgc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs11836625</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tgacccatccActtctgctgc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>It was indeterminate as to whether this polymorphism caused a measurable change in transcription.  It is suggested that it is not the causal polymorphism for lactase activity but may have some degree of association to the timing of downregulation of this gene among children.</comment>
<date>3-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>3-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment></comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3938</geneId>
<geneName>LCT</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>87</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>10573012</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000096</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>3-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tttttcatagatgtttcCatattgtttga</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tttttcatagatgtttcTatattgtttga</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>3-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>261 Japanese women subject.  82 had G allel, 48 had A allele, 131 were heterzygotic.  Bone mineral density (BMD) was 12% lower in lumbar spine (L2-L4) with the G allele compared to the C allele.</comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>G inhibition of binding weaker than A inhibition of binding in competition.</comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: Caco-2.  G allele activation was 30% less than A allele (with TK promoter fused to Cdx-2).  G allele activation was 15% less than A allele (with native hVDR promoter)</comment>
<date>3-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>7421</geneId>
<geneName>VDR</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>88</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>11450701</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GTAAAAACTTAT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000097</stableId>
<tfId>1045</tfId>
<tfName>CDX2</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>3-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>taggtcacaGtaaaaacttatttcttatt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs11568820</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>taggtcacaAtaaaaacttatttcttatt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>4-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HeLa (nuclear extracts).  Both shifted by nuclear extracts.  Binding greater in G allele than A allele.  Both less than canonical AP2 binding site.  Specific for AP2, unlabelled SP1 failed to exhibit this effect.</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>A allele associated on haplotype more common in responder group.  Direct association found with response to fluoxetine in response vs nonresponse.</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6532</geneId>
<geneName>SLC6A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>242</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15993855</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GCATCCCCCCTGCACCCCCAGCATCCCC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000313</stableId>
<tfId>7020</tfId>
<tfName>TFAP2A</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>4-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gcatcccccctgcacccccAgcatcccc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs25531</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gcatcccccctgcacccccGgcatcccc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Polymorphism nt is conserved only between human and chimp (against human, mouse, rat, dog, chimp comparison).</comment>
<date>4-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>4-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2 - HB8065.   -571 to +56 construct showed T allele decrease reported gene transcription by 38% (construct was extracted from patient with T allele).</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Complexes formed with T allele less intense than C allele constructs.  (Both constructs, noted in search space sequence, bound complexes)</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Addition of YY1 antibody removed complex 2 formation.</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6949</geneId>
<geneName>TCOF1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>243</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>16102917</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>atctgctggagatgagtaaaacgcagacccagccatcagagaattaacaag</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000314</stableId>
<tfId>7528</tfId>
<tfName>YY1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>4-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gagttcagagatgagtaaaacgcagaccCagccatcagagaattaacaag</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gagttcagagatgagtaaaacgcagaccTagccatcagagaattaacaag</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Tested GATA-1, -4, -6, Oct-1, HNF-3gamma, HNF-4alpha, RXR-alpha antibodies.  No change to EMSA or supershift.</comment>
<date>4-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>4-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Carriers of this polymorphism were associated with higher quinine metabolic ratio (higher CYP3A4 expression).  Population: 143 healthy, Tanzanians.</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Nuclear protein binds in close proximity to this polymorphism and the A allele has higher binding affinity than the G allele.</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1576</geneId>
<geneName>CYP3A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>279</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>16171783</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GAGACAAGGGCAGGAGAGAGGCGAT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000099</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>4-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gagacaagggcaAgagagaggcgatttaatagattttatgccaatggctc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2740574</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gagacaagggcaGgagagaggcgatttaatagattttatgccaatggctc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>4-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>In 334 case and 375 control individuals.  This polymorphism is associated to osteoarthritis.  </comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: OUMS-27 and Huh-7 cells.  In both lines, the C allele showed greater than 2 fold activity compared to the T allele.  (Search space sequence is -53 to +8 used in minimal construct)</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: Huh-7.  The T allele was more intense than the C allele.  (More factors bound to the T allele)</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>RNA Difference Plot analysis used in vivo.  The T allele showed decrease expression relative to C allele (1.09 difference)</comment>
<date>4-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00007</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00004</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>801</geneId>
<geneName>CALM1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>314</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15746150</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>gcgcaccatatatatatcgcggggcgcagactcgcgctccggcagtggtgctgggagtgtcg</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000146</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>4-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>atatatatcgcggggCgcagactcgcgctcc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs12885713</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>atatatatcgcggggTgcagactcgcgctcc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Tested supershift with anti-E2F-1 antibody.  Results unsuccessful. </comment>
<date>5-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>5-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Population: 42 Aspirin-induced asthma.  361 Childhood asthma; 313 adult atopic asthma; 88 adult non-atopic asthma.  Japanese.  Increased risk for AIA associated with C allele.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00010</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: HEK293 and HeLa cells.  Luciferase activity analyzed after 24hr of transfection.  C allele had significantly higher activity than T allele (33%-98% increase).</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: HEK293 and HeLa cells. In HEK293 cells, C allele band more intense than T allele band (21% increase) for nuclear factor complex.  Also observed in HeLa cells.  </comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>30009</geneId>
<geneName>TBX21</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>315</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15806396</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000100</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>5-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tgttccttaaggtacggagaaatggTgggtaaggtgttggggagg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs4794067</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tgttccttaaggtacggagaaatggCgggtaaggtgttggggagg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>5-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: K562 cells.  DNA-protein complex detected and competed with excess unlabelled WT probe.  Excess mutated probe (C allele) failed to compete with binding.  SP1 probe was shown to effectively compete binding whereas NFkappaB could not.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Anti-SP1 antibodies supershifted the G allele probe.  (anti-SP3 and anti-EKLF antibodies di not supershift)</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>B gal plasmid used.  Cell line: Jurkat and K562 cells.  (Construct region annotated as search space sequence; -759 to +3).  In Jurkat line, 40-fold expression difference for WT (G allele).  Tested SP1 positively for promoter activity.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>2235</geneId>
<geneName>FECH</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>316</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15850836</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GCGGCCTCCCGAGCCCTGAGTGCTGCCCTCAGCCCTCCCTTCTCCGCGACGCCCCTCGCCCGGTTGCTCGCAGCACCCCCAAGGCCGCTCCCCGAATCCCCCGGGCGCGAGGGCCCGGGCGCCAGCTGCCCGCTCTGCCCACGCCTTCTCAGGGATCCTGGCCCTGGCGGCCGCCGCGACAGACCCACTTACGCGGATCGCGGAGCAGGACGCCCGCGGCGCGCAGGGCCGCAGCCATGTTTGCGCCGAGTGAACGCATTGCCTGGGCAGCCTCGGCCCGAGTCCGGGCTCCTCCCGCGGCGGCGCGCCCAGGTGTCCGCCCAGCAGTGGCCGAGCCGGGTAGCGATCCCCACGCGCGTCCCCAGCCCCCTGACCTCGCGCCCTCCCGGCGCGCCCGCTCATTCGCTGCCGGGCCGGGGCGGGCGAGGCCAGGCAGAGACACGCCCCTCGCGGAGAGCCCGCCCCAGCTGGGCGCCGCTCCCTGCGTGAAAATGGGCCCGGGGGCTGAGCTAGAAGCCCGCTCCCCACCACCATCGCAGGTCACTGCAAAACCTGCTGGACTCCTAGTTGCGTGCCCTGTTTGCATCTGCCAAACTAGCGAAGTCAGGATCCTCAGCCATGACTCAGCAAATAACTTTTTTCGACGTTTCCATTACTATTATTTAGATATAAGGATGCTTTTGCCTCAGTTCTCCAGTTTGCCTGCCTAGTCACAACACAAGTGTGCAGATCCTGTTTTGTTTTGCTTTATTTTCAGAATAGA</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000101</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>5-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ggggagcgggcttctaGctcagcccccgggcc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ggggagcgggcttctaCctcagcccccgggcc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Polymorphism detected from 98 DNA samples 2.3kb upstream resequencing in Caucasian population.  </comment>
<date>5-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>5-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2, Rat hepatocyte, Human hepatocyte. Increased promoter activity with C allele. (Construct annotated as search sequence space)</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>C allele detected a protein-complex band.    T allele did not.  Incubated with C/EBP protein.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Incubated with TBP.  C allele had weaker binding than T allele.  Suggesting a TATA box is altered and a C/EBP box is created.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Shorter transcripts dominate in C allele compared to T allele (longer transcripts).  This is due to increased affinity for the TATA box at the -82 polymorphic site.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00020</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00004</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1555</geneId>
<geneName>CYP2B6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>317</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15722458</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>TTAATTAGTGGCCACATGCAGCAAGTGACTATCACATTGGACAATGTAGCCCCAACCCACTGTATGACCTTGGGTAAGACTTGCAAACTGTCATTGCTTCAATATCTCCATCTATAAAATGGGGATGGCAACAATACCTCACTAAGAGTGTAAAGACTGAGTTACTGTGTGTAAAGCACTTCACGCCTCCCCATCGGTGCTTCACCCTGGGGCTGCAATGAGCACCCAATCTTAGTGTCAGATGACACAGCACAGCAAGACCGAGGCCCTTGGTTCAGGAAAGTCCATGCTGCCACCTCTTCAGGGTCAGGAAAGTACAGTTTCCACCTCTTACAAATAGGACTGTTTGTCTGCTCCTCCTGGGTCAAAGTAACTTCGGGTTCAGGTCCTGGATCCAGCAAAGGGTTTGCTTAACATTGCAAGAAAGATGTTGCCTCATGGTCAAAAGTCAGGCGTAGGATGAGACAGGCAGACACGCACACATTCACACCCACGTTTTGCAAAGATGGACTGACCCTGTCAGAGGATGTGTGGGTGAAGGTGCACAGTGAGGATAGAGACATATGGGAGTCCAGTAGACATCAATCAAACTGGACTCAGTTTGCACACACCTGGAGCTCAAGAGTCTCCAGGGGGAAAACAGAGACACAAAGTCAGACAGAGAGAGAGCCAGAGAAATTTCCTGCACCGTGAAGATAGTCAGAGGCAGGGAAGAAACTCCTTAGCACTAGTTAGAGTGATCAGAAACCAAGAGGACCTGATCGCTGTACCTGCCAGGTCTCAGTTTCTGTCTCCTTCCAACTGACCACCTCTTCCTCTGAGACTCACCAGTTCTGCATCTCTTGCTCCTCCTTCTGTTTCTCCGACCACTTCCACCTGTGGCTGTCACAGAAGGGCGGATGAAGGAGGGGACACTGGAGATAGACTCAGCATCTGCAGGCTTCCAAAGAGAGGGGCTAGGAGATCCACCAACACACCAGCACAAATACACCAGCACACACAGATACACACAATTGGTTCATGTATTGCTAGGTTACAGTTTGCTATGCTACAAAGGCAGTAGGCCAAATTTGATTGAATTGAATAATTCCTTATTTTCATCAGCTTCTCCTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTATTGCTGTGTCACCCAGGCTGGAGTGCAGTGGTGTAATCTTGGCTCACTGCAGCCTCCACCTCCCAGGTTCAAGTGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTAAAAGTACCCACCATCACGCCCGGTTAATTTTTGTGTTTTTAGTACAGATGGGGTTTTGCCATGTGGGCCAGGATGGTCTCGAACTCTTGACCTCAATTGATCTGCCCCCCTCAGCTTCCCAACGTGCTGGGATTACAGGTGTGAGCCACCGCACCCAGCCAGCCTCTCAGTTTTGAACATGCACTACCACCACCTCCACAACACACAAATGTAAATGCACTTTCGTATATAAAACTGTATAAATACAAGGAAGCTCATACACATGCAAGGATACACACATAAGCACCCCCAGATTCAACCACAGAAATATACGCCAGTACATTTGCATAAATTCAAACACCCCTTTACATGTAAAAATCATATAAGCACATACAGGGATGCAAGCAGGCATGGACAAATGCATGCAAGCACAGACAAACAGACAAAGCTAAGTAAAAAAGTGCAAGCTCACCTATGCTTACAAAAATAGACATACATATACCCACAAACCCACACACCCACACATTCACTTGCTCACCTGGACTTTGATATCTCTACCACTGTATCCCTGCCAATATCTACAGAGTGGGTAAAGGGATAGGCATCAGGTCACTGGGTTGCCCAAGCAGGAAGTCTGGGTTCCCTAACAACTTTTTCTAAGCTAATGCTCCTGGATGATGATGAAAAAGGAGGTGGGGAATGGATGAAATTTTATAACAGGGTGCAGAGGCAGGGTCAGGATAAAAGGCCCAGTTGGAGGCTGCAGCAGGGTGCAGGGCAGTCAGACCAGGACCATG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000102</stableId>
<tfId>TBP / C-EBP</tfId>
<tfName>TBP / C-EBP</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>5-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>aggtggggaatggatgaaatttTataacagggtgcagaggcagggtcagg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>aggtggggaatggatgaaatttCataacagggtgcagaggcagggtcagg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>5-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HeLa and HUVEC.  T allele demonstrated weaker shifts than C probe.  Competition with unlabelled competitor demonstrated 10-fold greater affinity for C compared to T allele.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Nuclear extracts from HUVECs used.  Antibodies for SP1. Sp2, Sp3, and Sp4 used.  Supershift of both Sp1 and Sp3 detected.  Experiment confirmed in C11STH, HeLa, and NT2 cell lines. </comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Search space sequence is the -7137 to -8087 (950bp) construct.  Cell line: HeLa.  C allele had higher promoter activity for all tested retinoic acid concentrations.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>5327</geneId>
<geneName>PLAT</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>318</id>
<lociName><![CDATA[
Retinoic acid & Steroid Hormone Enhancer]]>
</lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15466927</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGAACTCAAGGTATCCGCCTGCCTTGGCCTCCTAAAGTGCTGAGATTACAGGCATGAGCCACTGTGCCCAGCCTACTCCTTATTTTAAATGTGCAAACTCTGCAAAGTGGCTGTGCTGAGGCACTTCCAAATGCCACCCAGGTGGTGCTCAAGCTCTGGTTTCTGCTCTATGAGCCCTTCTTCTTCTGGACCTGGTGCCACCAACCCTTGCAGCCTCCTATGGAGGATGGTGCGTGTTTCCTTTCAGCCTTTCTGGTCATTTCTTTTCTTGTTTTAAAATAACAACACCAGGCCAGGTGAGGTGGCTCACTCCTGTAATCCTAACACTTTGGGAGGCCAAGGTGGGAGGATTCCTTGAGCCCAGAAGTTTGAGACCAGCCTGGGCAACATGGCGAGACCCTATCTCTACAAATAATTAAAAAATTAGTCAGGTGTGGTGGCACATGCATGTAGTCCCAGCTACTTAGGAGGCTGAGGTGGAAGGATCCCTTGAACCTGAAAATTTGAGGTTGCAGTGAACTGTGATCCCATCACTGCACTCCAGCCTGGGAGACAGAGTAAAAGCCTGTCTCTAAAAATAAAAAATAAATAAACACATAAATAACACTGACAATAACCAAAACCAAGTGAATACAGATAATTCCTTCTGACCCCAGGGTGACCCCAGAGTCCCAGGCCATGGCTGTGTCTGGGGCAGGCTCCTTTGGGAGAGCGGCCAAAGCCCTATTCACCTCGGCAATGAGATCACTCAGACCTGGGGGGAGGCGCGTTCTGGGAGAGCGTGGTGACTTCCACAGCAGGGGCTCTTGCATCAGTTCTGGTTACCCACGGGAGACTGCATGTGCTCAGGGTGACAGGAACACCACTGTTTACATGGGACCCACCTCCCGCCATGGCATCACAGGACTCG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000103</stableId>
<tfId>Sp1 / Sp3</tfId>
<tfName>Sp1 / Sp3</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>5-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gctttggccgctctcccaaaggagccTgccccagacacagccatggcc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2020918</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gctttggccgctctcccaaaggagccCgccccagacacagccatggcc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Identified in 56 Italian individuals.  T(0.78)/G(0.22) </comment>
<date>5-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>5-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: U2OS, COS7, and HeLa cell lines.  T allele had higher affinity than G allele.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Supershift removed with addition of anti-Sp1 and anti-Sp3 antibodies.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>(Construct annotated as search sequence space -474 to +42).  G allele had lower expression activity.  Cotransfection with Sp1 overexpression also demonstrated higher affinity of T allele.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6696</geneId>
<geneName>SPP1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>319</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>15479859</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>TAAGCTTGAGTAGTAAAGGACAGAGGCAAGTTTTCTGAACTCCTTGCAGGCTTGAACAATAGCCTTCTGGCTCTTCAATAAGTACAATCATACAGGCAAGAGTGGTTGCAGATATTACCTTTATGTTACTTAAACCGAAAGAAACAAAAATCCATTCTATTTAATTTTACATTAATGTTTTTCCCTACTTTCTCCCTTTTTCATGGGATCCCTAAGTGCTCTTCCTGGATGCTGAATGCCCATCCCGTAAATGAAAAAGCTAGTTAATGATATTGTACATAAGTAATGTTTTAACTGTAGATTGTGTGTGTGCGTTTTTGTTTTTTTTTGTTTTAACCACAAAACCAGAGGGGGAAGTGTGGGAGCAGGTGGGCTGGGCAGTGGCAGAAAACCTCATGACACAATCTCTCCGCCTCCCTGTGTTGGTGGAGGATGTCTGCAGCAGCATTTAAATTCTGGGAGGGCTTGGTTGTCAGCAGCAGCAGGAGGAGGCAGAGCACAGCATCGTCGGGACCAG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000104</stableId>
<tfId>Sp1 / Sp3</tfId>
<tfName>Sp1 / Sp3</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>5-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ctcatgacacaatctcTccgcctccctgtgttggt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ctcatgacacaatctcGccgcctccctgtgttggt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Background controlled by using site-directed mutagenesis.</comment>
<date>5-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>5-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment><![CDATA[
Cell line: HLF-1.  Site-directed mutagenesis used to create SNP.  Extracted from clone 973 M2 from library RPCI5 (Sanger Center Clone Resource Group).  (Search sequence space is annotated with construct -1811 to + 108).  C allele had lower expression activity than G allele (28%+/-3% P<0.005).  This was repeated in serum-stimulated (31% lower).]]>
</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>173 bypass patients (GG=115, GC=56, CC=2) vs 454 health caucasian controls.  Associated to phenotype: lower CRP levels (C-reactive protein) with C allele.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00000</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00011</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00006</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>5743</geneId>
<geneName>PTGS2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>320</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12377741</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>AAGTCGGAGTACTGGGATAGACCCAGGAGGTCAGAGCGGAAACTCTGCCCGGGTGCGTGGAACCGGAGTCCCCGGTGCGCGGCGCCAGGTACTCACCTGTATGGCTGAGCGCCAGGACCGCGCACAGCAGCAGGGCGCGGGCGAGCATCGCAGCGGCGGGCAGGGCGCGGCGCGGGGGTAGGCTTTGCTGTCTGAGGGCGTCTGGCTGTGGAGCTGAAGGAGGCGCTGCTGAGGAGTTCCTGGACGTGCTCCTGACGCTCACTGCAAGTCGTATGACAATTGGTCGCTAACCGAGAGAACCTTCCTTTTTATAAGACTGAAAACCAAGCCCATGTGACGAAATGACTGTTTCTTTCCGCCTTTTCGTACCCCCCACAAATTTTTCCCTCCTCTCCCCTTAAAAAAATTGCGTAAGCCCGGTGGGGGCAGGGTTTTTTACCCACGGAAATGAGAAAATCGGAAACCCAGGAAGCTGCCCCAATTTGGGAGCAGAGGGGGTAGTCCCCACTCTCCTGTCTGATCCCTCCCTCTCCTCCCCGAGTTCCACCGCCCCAGGCGCACAGGTTTCCGCCAGATGTCTTTTCTTCTTCGCAGTCTTTGCCCGAGCGCTTCCGAGAGCCAGTTCTGGACTGATCGCCTTGGATGGGATACCGGGGGAGGGCAGAAGGACACTTGGCTTCCTCTCCAGGAATCTGAGCGGCCCTGAGGTCCGGGGGCGCAGGGAATCCCCTCTCCCGCCGCCGCCGCCGTGTCTGGTCTGTACGTCTTTAGAGGGTCGAGGAAGTCACGTCGGGACAGACTGGGGCGAGTAAGGTTAAGAAAGGCTGACATGTTTTATGTTTTAGTGACGACGCTTAATAGGCTGTATATCTGCTCTATATGCAGCACATACATACATAGCTTTTTAAAAAACTCTTATTTTGTGGAATGAAATAGCTACCTTCAGTGTACATAGCTGTAATTTATCTTTGTAGCTAAGTTGCTTTCAACAGAAGAAATACTGTTCTCCGTACCTTCACCCCCTCCTTGTTTCTTGGAAAGAGAGGCGGGAAAGGTAAATTCTCCTCATAATACTGGTCCTAAGCAGTTACCCTGTAAATAGTTAATGTGAGCTCCACGGGTCACCAATATAAAGTTTCCTGCCTTCTGATGGACAAAGGAAGCGGCGATGGCCAGAATTTGCAGGGACGCTAAATGTCCAAAACGTATGCCTTAAGGCATTTCTCTCCCTGATGCGTGGATTATTTTGGTTACTAGCCCTTCATAGGAGATACTGGTAAAATAAATTCGAGTTTTAAAGTTCACTCTTTTGTCTTTTCTGTCCACTTTTCCAAGATTATGAGTTGTGACCATGGATCAAAGTACAACATAGCATTTACTTTTCAGTTGCCTGGGCTTATTGGGGCTAATTTTCTATTCTCGTTTTGGAACATAGTTGGATGAGGAATTAATTAGATGGAAGGGAGATTTTGACAGTTGGAATTTCATCTTTGCTTTTGTTTAACATCTATCATGGGTAGTGCTCAGGGAGGAGCATGTGAGGGTGAGATACTAAAAAATATATATATGTATATGTGTGTGTGTATATATACATATATATATACACACACACCAGAAAAGAAGTGGAAAATAGAAAATTCAGTTATGTCCTAAGTCCTTAGCATTACAGGAAAATGACAGCATAAAACCTGAAATAAAACTACACCAGGTACCTCAATTTGTAGAAGTCTTATAAGAAAAAAATAAATAAGAGACTCACTTGGAGGTTTTTTTTTTAACTGTTTTGCTTAGTGTACACATCTGATTCTTCATGAGACACGGATGACTAAAATTCCATCTCATCTAGGAAGCCTTTCTCCTCCTCTAGTCATATTTCATCATTCCATTTATGGCACTCCTATTTATTGCATGGAATCTTAC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000105</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>5-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>attatgaggagaatttacctttcccGcctctctttccaagaaacaagg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs20417</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>attatgaggagaatttacctttcccCcctctctttccaagaaacaagg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
</commentSet>
<dataset></dataset>
<date>5-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: Jurkat.  A allele binds a unique complex compared to G allele.  Similar activity tested in Raji, HepG2, HeLa, and U937 cell lines.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: Jurkat cells.  In Jurkat, G allele cause 3 fold repression of SV40 promoter activity.  In U937, in double copy, G allele causes 1.95fold enhancement of activity (against control).  A allele generally increased transcription 2-fold higher than G allele.  Site-directed mutagenesis used to control background.</comment>
<date>5-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>7124</geneId>
<geneName>TNF</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>321</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>9293772</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000106</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>5-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gttttcaggggcatgGggacggggttcagcctccagggt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs1800629</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gttttcaggggcatgAggacggggttcagcctccagggt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This mutation was suggested to counteract the decreased expression effects of a linked (AT)n repeat polymorphism.</comment>
<date>6-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>6-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: Jurkat, THP-1 cell line.  Mutagenesis used to introduce variants into construct (329-bp fragment, genomic DNA).  T allele associated with higher activity (8.13 +/ 0.46 vs 6.87 +/- 0.49).</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1493</geneId>
<geneName>CTLA4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>322</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12058260</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000107</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>6-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ctccaagtctccacttagttatccagatcctCaaagtgaacatgaagcttcagtttcaaa</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs5742909</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ctccaagtctccacttagttatccagatcctTaaagtgaacatgaagcttcagtttcaaa</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Cross-referenced in rSNP_DB as rSNP00J0001.
http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+EnIK1R58CA+-e+[rSNP_DB:'rSNP00J0001']
Binding tested as mutually exclusive between HNF-1 and HNF-6.</comment>
<date>6-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>6-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>HNF-6 bound DNA.  This was competed successfully with probe possessing the canonical HNF-6 binding site.  Also tested in Cell line: COS-7.  Competed binding of complex with addition of probe possessing the HNF-6 binding site.  </comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Supershift of HNF-6 by anti-HNF-6 antibody.  </comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>C allele had reduced affinity for HNF-6 complex.  This binding could be competed by T allele.</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2 and COS-7.  C allele had reduced activity and transactivation by HNF-6 was abolished.  </comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>5624</geneId>
<geneName>PROC</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>323</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>9553065</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000108</stableId>
<tfId>3175</tfId>
<tfName>ONECUT1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>6-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>caagcaaatatttgtggttatggaTtaactcgaactccaggctgtcatgg</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>caagcaaatatttgtggttatggaCtaactcgaactccaggctgtcatgg</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Allele was shown to associate to cebral malaria in African population (OR 4.6, 95% CI 1.3-15.7, P=0.016).  Cross-referenced in rSNP_DB as rSNP00J0002.  
http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+EnIK1R58CA+-e+[rSNP_DB:'rSNP00J0002']</comment>
<date>6-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>6-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: MonoMac6.  Detected protected region from -404 to -374</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00015</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00003</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Complex binding detected.  Was competed only by A allele probe.</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Complex formation was inhibited by oligonucleotide probes corresponding to Oct-1 binding site.</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Supershift with antibodies against Oct-1.</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: MonoMac6 cells.  Used 1.2kb promoter sequence (annotated as search space sequence).  Used site-directed mutagenesis to introduce A mutation.  A allele showed 35% increase in expression compared to G allele.</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>7124</geneId>
<geneName>TNF</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>324</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>10369255</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>GAGGGACAGAGGGCTCAAAGGGAGCAAGAGCTGTGGGGAGAACAAAAGGATAAGGGCTCAGAGAGCTTCAGGGATATGTGATGGACTCACCAGGTGAGGCCGCCAGACTGCTGCAGGGGAAGCAAAGGAGAAGCTGAGAAGATGAAGGAAAAGTCAGGGTCTGGAGGGGCGGGGGTCAGGGAGCTCCTGGGAGATATGGCCACATGTAGCGGCTCTGAGGAATGGGTTACAGGAGACCTCTGGGGAGATGTGACCACAGCAATGGGTAGGAGAATGTCCAGGGCTATGGAAGTCGAGTATGGGGACCCCCCCTTAACGAAGACAGGGCCATGTAGAGGGCCCCAGGGAGTGAAAGAGCCTCCAGGACCTCCAGGTATGGAATACAGGGGACGTTTAAGAAGATATGGCCACACACTGGGGCCCTGAGAAGTGAGAGCTTCATGAAAAAAATCAGGGACCCCAGAGTTCCTTGGAAGCCAAGACTGAAACCAGCATTATGAGTCTCCGGGTCAGAATGAAAGAAGAAGGCCTGCCCCAGTGGGGTCTGTGAATTCCCGGGGGTGATTTCACTCCCCGGGGCTGTCCCAGGCTTGTCCCTGCTACCCCCACCCAGCCTTTCCTGAGGCCTCAAGCCTGCCACCAAGCCCCCAGCTCCTTCTCCCCGCAGGGACCCAAACACAGGCCTCAGGACTCAACACAGCTTTTCCCTCCAACCCCGTTTTCTCTCCCTCAAGGACTCAGCTTTCTGAAGCCCCTCCCAGTTCTAGTTCTATCTTTTTCCTGCATCCTGTCTGGAAGTTAGAAGGAAACAGACCACAGACCTGGTCCCCAAAAGAAATGGAGGCAATAGGTTTTGAGGGGCATGGGGACGGGGTTCAGCCTCCAGGGTCCTACACACAAATCAGTCAGTGGCCCAGAAGACCCCCCTCGGAATCGGAGCAGGGAGGATGGGGAGTGTGAGGGGTATCCTTGATGCTTGTGTGTCCCCAACTTTCCAAATCCCCGCCCCCGCGATGGAGAAGAAACCGAGACAGAAGGTGCAGGGCCCACTACCGCTTCCTCCAGATGAGCTCATGGGTTTCTCCACCAAGGAAGTTTTCCGCTGGTTGAATGATTCTTTCCCCGCCCTCCTCTCGCCCCAGGGACATATAAAGGCAGTTGTTGGCACACCCAGCCAGCAGACGCTCCCTCAGCAAGGACAGCAGAGGACCAGCTAAGAGGGAGAGAAGCAACTACAGACCCCCCCTGAAAACAACCCTCAGACGCCACATCCCCTGACAAGCTGCCAGGCAGG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000110</stableId>
<tfId>5451</tfId>
<tfName>POU2F1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>6-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tgaagcccctcccagttctagttctatctttttcctgcatcctgtctggaaGttagaaggaaacagacca</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs1800750</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tgaagcccctcccagttctagttctatctttttcctgcatcctgtctggaaAttagaaggaaacagacca</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>rSNP_DB crossreferenced: rSNP00J0003
http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+EnIK1R58CA+-e+[rSNP_DB:'rSNP00J0003']</comment>
<date>6-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>6-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HEL cell line.  C allele had more CAT activity.  In G allele, the activity was reduced by 84% (+/- 13%).  (Construct is annotated as search space region).</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00019</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Used 24-mer sequence, TGTGCTATCTGCCGCTGCAGCGCG.  Nuclear extracts from CHRF-288, HEL, or HeLa cells.  Protein bound to C allele but not G allele.   C allele could not be competed off by less than 35-fold excess of unlabelled oligo-nt whereas 1.5-fold excess could compete off G allele.</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Supershift detected with monoclonal antibody to GATA-1 not with GATA-2.</comment>
<date>6-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>2812</geneId>
<geneName>GP1BB</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>361</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>8703016</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>TTGTGAATGCCGCGTCCTGTCCTGGTGACAGGAGAACAATGTTGGTGAACGTCGCAGCGGGTGTCCGAGTGCTCCGTGTGCCCCTGAGAGCGGGTGGGAGCGGAAGCCTGAGCGGCCTGCGGCCTCCGGCGATAGTGTGCTATCTGCCGCTGCAGCGCGCGTCCGCGCGGCCTCTGGGCTATTTCTGGCCAGGCCGCAGCACTGTGGTCGGTGCGGGCGTGGCAGGGGCGGGGCGGCCTTATCGCTCGGCTCTCCCGCCTACGCCTCCCGCTGCAGAGTAAGCCGGGCTGCCGTCTTCTCGCCATGGGCTCCGGTGAGTCTGGAGTCCGGTCGGGCCCCCGGCTGCTCCCTAGGCCGACCCGGGTTGAGAGGAGCTCTGGTCGTT</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000363</stableId>
<tfId>2623</tfId>
<tfName>GATA1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>6-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ccggcgatagtgtgctatCtgccgctgcagcgcgcgtcc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ccggcgatagtgtgctatGtgccgctgcagcgcgcgtcc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This polymorphism is close to rs13434811 which has a reduced yet similar affect on YY1 binding.
rSNP_BIB Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0J0004']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Rat liver nuclear extract.  A thrid complex binding the oligonucleotide was abated with the A allele compared to the WT G allele.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Tested HNF3, GATA, HNF1, C/EBP, Sp1, AP1, SRE, and ANF.  SRE in 40-fold excess competes protein band formation.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>anti-YY1 causes supershift with protein complex.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6999</geneId>
<geneName>TDO2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>393</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>10580097</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>TGCCAAATAATGGCAGATAAGAATAGGGAG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000403</stableId>
<tfId>7528</tfId>
<tfName>YY1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ttatatataatgccaaataatgGcagataagaatagggagaaaaagaattacaaagctaa</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs16998970</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ttatatataatgccaaataatgAcagataagaatagggagaaaaagaattacaaagctaa</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This polymorphism is within 3 bases of rs16998970 which has a greater affect on YY1 binding.
rSNP_BIB Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0J0004']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Rat liver nuclear extract.  A third complex binding the oligonucleotide was decreased with the T allele compared to the WT G allele.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Tested HNF3, GATA, HNF1, C/EBP, Sp1, AP1, SRE, and ANF.  SRE in 40-fold excess competes protein band formation.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>anti-YY1 causes supershift with protein complex.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6999</geneId>
<geneName>TDO2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>394</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>10580097</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>TGCCAAATAATGGCAGATAAGAATAGGGAG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000404</stableId>
<tfId>7528</tfId>
<tfName>YY1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ttatatataatgccaaataatggcaGataagaatagggagaaaaagaattacaaagctaa</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs13434811</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ttatatataatgccaaataatggcaTataagaatagggagaaaaagaattacaaagctaa</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This was a cuasative allele of HPFH (hereditary persistence of fetal hemoglobin) in a Japanese family based on linkage and resequencing analysis. 
rSNP_BIB Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0J0006']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HeLa, RPMI, K562, KU812, and MEL cells.  In all extracts, C allele had two shifted bands, T allele had one.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Competed binding with CP1 oligo-nt.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Protection pattern showed that binding of Cp1 is higher affinity to distal CCAAT motif.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00015</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00003</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3048</geneId>
<geneName>HBG2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>395</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>1698280</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>CATGGGTTGGCCAGCCTTGCCTTGACCAATAGCCTTGACAAGGCAAACTTGACCAATAGTCTTAGAGTATCCAGTGAGGCCAGGGGCC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000405</stableId>
<tfId>50820</tfId>
<tfName>CP1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>cttccccacactatctcaatgcaaatatctgtctgaaacggtccctggctaaactccacccatgggttggccagccttgccttgacCaatagccttgacaaggcaaacttgaccaatagtcttagagtatccagtgaggccaggggccggcggctggctagggatgaagaataaaaggaagcacccttcagcagttccacacactcgctt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>cttccccacactatctcaatgcaaatatctgtctgaaacggtccctggctaaactccacccatgggttggccagccttgccttgacTaatagccttgacaaggcaaacttgaccaatagtcttagagtatccagtgaggccaggggccggcggctggctagggatgaagaataaaaggaagcacccttcagcagttccacacactcgctt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Mutation detected in French-Canadian patient with low-levels of VII:Ag and VII:C.  rSNP_BIB Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0J0007']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2.  Transfected +1 to -185 sequence (annotated as search space sequence).  Mutant promoter (G) allele exhibited 5.8 +/- 2.2% of WT promoter activity.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: HeLa.  Oligo-used GTGTCCTCCCCTCCCCCATCCCTCT.  Binding to SP1 oligo could be competed away with WT oligo but not mutant oligo.  </comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>2155</geneId>
<geneName>F7</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>396</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>9716591</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>AGTGGCTGGGCAGCAGGGGATGCATGGCCACTGGCCGGCCAGGTGCAGCTCTCAGCTGGGGTGTTCAGAGGACGCCTGTGTCCTCCCCTCCCCCATCCCTCTGTCACCCTTGGAGGCAGAGAACTTTGCCCGTCAGTCCCATGGGGAATGTCAACAGGCAGGGGCAGCACTGCAGAGATTTCATCA</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000406</stableId>
<tfId>6667</tfId>
<tfName>SP1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gaggacgcctgtgtcctcccctccCccatccctctgtcacccttggaggcagagaacttt</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gaggacgcctgtgtcctcccctccGccatccctctgtcacccttggaggcagagaacttt</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Tested unsuccessfully, AP1 and NF-E2 as transcription factors.  Polymorphism was found in Sardinian pedigree for Delta-thalassemia; was not found in larger population (90 chromosomes).  </comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HeLa and noninduced and DMSO (dimethyl sulfoxide)-induced K562 cells.  Mutant A allele displays higher affinity for erythroid-specific binding.  </comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3045</geneId>
<geneName>HBD</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>397</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>1309671</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>CTCTACAGATAGGGAGCA</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000407</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gtaagaaggttcctgaggctctacagataGggagcacttgtttattttacaaagagtacatgggaaaaga</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gtaagaaggttcctgaggctctacagataAggagcacttgtttattttacaaagagtacatgggaaaaga</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Mutation only detected in 3 Japanese delta-thalassemia patients.  Not detected in 58 healthy Japanese.
rSNP_Bib Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0M0010']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: MEL (mouse erythroleukemia).    GATA-1 binds to normal (T allele) and mutant (C allele) weakly.  This binding was competed out by canonical GATA-1 oligo.  WT probe: ATGAAACCCTGCTTATCTTAAACCAACCTG.  MT probe: ATGAAACCCTGCTCATCTTAAACCAACCTG</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment><![CDATA[
Cell line: MEL cells.  WT activity was 19.7 +/= 2.1  whereas mutant activity was at background level (<1.0%).  Plasmid sequence annotated as search space sequence.]]>
</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00019</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3045</geneId>
<geneName>HBD</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>398</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>1515647</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>TCTGCCCTGCCTTTTATGCTGGTCCTGTCCTCCCTGCTCCAGTGAGCAGGTTGGTTTAAGATAAGCAGGGTTTCATTAGTTTGTGAGAATGAAAAATGAACCTTCATTCCACTATTCCCTTAACTTGCCCTGAGATTGGCTGTTCTGTCATGTGTGTCTTGACTCAGAAACCCTGTTCTCCTCTACATATCTCCCCACCGCATCTCTTTCAGCAGTTGTTTCTAAAAATATCCTCCTAGTTTCATTTTTGCAGAAGTGTTTTAGGCTAATATAGTGGAATGTATCTTAGAGTTTAACTTATTTGTTTCTGTCACTTTATACTAAGAAAACTTATCTAAAAGCAGATGTTTTAACAAGTTGACTCAATATAAAGTTCTTCTTTGCCTCTAGAGATTTTTGTCTCCAAGGGAATTTTGAGAGGTTGGAATGGACAAATCTATTGCTGCAGTTTAAACTTG</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000408</stableId>
<tfId>2623</tfId>
<tfName>GATA1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>tttttcattctcacaaactaatgaaaccctgctTatcttaaaccaacctgctcactggagcagggaggac</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>tttttcattctcacaaactaatgaaaccctgctCatcttaaaccaacctgctcactggagcagggaggac</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>rSNP_BIB Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0M0010']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>40bp 5' sequence + 36bp of first exon were transfected and showed increased (15-20 fold) activity with estrogen treatment.  This demonstrated the presence of an ERE (Estrogen-Responsive Element).</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00019</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Used WT oligo, protein complex bound.  Was supershifted with anti-ER.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2.  Cotransfection of alleles. C allele has reduced activity compared to A allele (~16-fold reduction).  Under Beta-estradiol treatment</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00019</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Looked at basal transcription.  C allele has 2 to 3-fold increase over A allele.  Suggested role of MLTF binding.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00019</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2.  C allele bound stronger complex.  This was competed out with MLTF oligos.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>MLTF antibody supershifted competed by C allele.  No supershift with non-specific antibody NF-1.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Cotransfection with MLTF expression vector. C had 3- to 4-fold increase compared to A allele.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00019</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>183</geneId>
<geneName>AGT</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>399</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>9931090</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000409</stableId>
<tfId>ERE / MLTF</tfId>
<tfName>ERE / MLTF</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>ccccacccctcagctataaatagggcAtcgtgacccggccgggggaagaagctgccgttgttctgggtac</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs5050</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>ccccacccctcagctataaatagggcCtcgtgacccggccgggggaagaagctgccgttgttctgggtac</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Mutation observed in 3 black individuals possessing the Fy(a-b-) phenotype.  Not found in 100 randomly-selected Duffy + Japanese.
rSNP_BIB Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0J0014']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HEL and HMvEC cells.  HEL cells showed disrupted promoter activity for C allele vs T allele.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00019</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Supershifted by anti-GATA-1 in HEL cell.  The probe is annotated as the search space sequence.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>2532</geneId>
<geneName>FY</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>400</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>8651934</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>CCCTCATTAGTCCTTGGCTCTTATCTTGGAAGCACAGGCGCTGACAGCCGTCCCAGCCCTTCTGTCTGCGGGC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000410</stableId>
<tfId>2623</tfId>
<tfName>GATA1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>gcgtggggtaaggcttcctgatgccccctgtccctgcccagaacctgatggccctcattagtccttggctcttaTcttggaagcacaggcgctgacagccgtcccagcccttctgtctgc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs2814778</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>gcgtggggtaaggcttcctgatgccccctgtccctgcccagaacctgatggccctcattagtccttggctcttaCcttggaagcacaggcgctgacagccgtcccagcccttctgtctgc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>rSNP_BIB Cross-reference: http://srs6.bionet.nsc.ru/srs6bin/cgi-bin/wgetz?-id+2eRHV1R75Ax+-e+[rSNP_BIB:'RFrSNP0J0015']</comment>
<date>11-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>11-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HeLa and K562 cells.  G allele enhanced the intensity of binding.</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>anti-SP1 supershifted protein-DNA binding complex in mutant allele not WT allele (C allele)</comment>
<date>11-Oct-2005</date>
<evidenceClassStableId>OREGEC00002</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00002</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3048</geneId>
<geneName>HBG2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>401</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>1688466</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0000411</stableId>
<tfId>6667</tfId>
<tfName>SP1</tfName>
<tfSource>NCBI</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>11-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>cagcagtatcctcttgggggcCccttccccacactatctcaatgcaaatatctgtctgaa</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>cagcagtatcctcttgggggcGccttccccacactatctcaatgcaaatatctgtctgaa</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This polymorphism was chosen because of disconcordant frequencies in african and european populations at this position.</comment>
<date>31-Oct-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset></dataset>
<date>31-Oct-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell line: HepG2 (used nuclear extract).  Bound strongly to G allele compared to T allele probe.  T probe labelled as search space sequence.</comment>
<date>31-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00001</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
<evidence>
<cellType></cellType>
<comment>Each probe was competed with an unlabelled competitor (the probe with the alternative allele).  Differential binding patterns were observed.</comment>
<date>31-Oct-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00003</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00001</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>80781</geneId>
<geneName>COL18A1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>1997</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>16229994</reference>
<scoreSet>
<score>
<date>1-Nov-2005</date>
<score>1</score>
<userName>obig</userName>
</score>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>search_space</internalSequenceType>
<sequence>AGACTGAGGCCGGGAAGGAGTATGCATTCCTGCCCTGGTCC</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0001732</stableId>
<tfId>UNKNOWN</tfId>
<tfName>UNKNOWN</tfName>
<tfSource>USER DEFINED</tfSource>
<tfVersion></tfVersion>
<type>REGULATORY POLYMORPHISM</type>
<variationSet>
<variation>
<date>31-Oct-2005</date>
<referenceSequence>
<end>0</end>
<internalSequenceType>reference_sequence</internalSequenceType>
<sequence>accggatccttttgtggacggggagactgaggccgggaaggagTatgcattcctgccctggtcccgggctccgtctctgc</sequence>
<start>0</start>
<verified>false</verified>
</referenceSequence>
<regulatoryVariationCrossReferenceSet>
<regulatoryVariationCrossReference>
<snpId>rs755548</snpId>
<source>dbSNP</source>
</regulatoryVariationCrossReference>
</regulatoryVariationCrossReferenceSet>
<type>GERMLINE</type>
<variantSequence>
<end>0</end>
<internalSequenceType>variant_sequence</internalSequenceType>
<sequence>accggatccttttgtggacggggagactgaggccgggaaggagGatgcattcctgccctggtcccgggctccgtctctgc</sequence>
<start>0</start>
<verified>false</verified>
</variantSequence>
</variation>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: testis derived transcript (3 LIM domains).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.416502947  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 5.178597039  HeLa: 5.717058082  HT1080: 4.884851538  MRC5: 3.291587284  JEG3: 5.993174926  U87: 4.504337514  G402: 3.818663379  HCT116: 5.774321884  CRL1690: 3.927734702  AGS: 5.642756966  Panc1: 4.064194284  HMCB: 4.253541987  MG63: 3.406070104  Snu-182: 3.747317265.  Number of positive cell lines: 14.  Mean: 28.17177311.  Mean(log): 4.586014783.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>26136</geneId>
<geneName>TES</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>1998</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CCTGAGAATTTTAGTCGCAAGGAATGAAAAAAACTGTTTTCTCATTTCGAGTTTTTATTGGTCAATAGCTTCCTAACCGAAAACTCTGCAGTCCTAACACAATATTTTGTATCCATTTTCAAAAATCCAGTTCTGGGCATAAAATAGAATTAATGCTCAAGTCAAAAACTTTGTGTTTAGAAGATAAAATATTAGGAACCATGAGTATGAGAAAAACAAAAACTGTTTTCTGTATTTTTCCCTTCCTCTCTCTGCAAAACTTCTCTATTTGATAAGGGACAGCTAGCTTAAATTTACCACAAAGTAAAACATGAGCAAATCCCCTGGAACGAGGAGAACTTTCGCACAGGGCAATTCACTCGAATGTGACATCAGCATTCCTTCTGAGTCATAGTCTGGTCCCCACCCTTTTCTCCCAGGCGACACCAGGCTCCGCATAACCCGGGAGTGGCTCAGGTAGGGCCGTCGGTTCCAGTGCCTGCGAGGCAGCAGCCAAGCTGAAAATGTCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003433</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "capping protein (actin filament) muscle Z-line, alpha 2".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.559414991  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 6.108844296  HeLa: 4.138436445  HT1080: 4.871262384  MRC5: 3.910455679  JEG3: 4.215337692  U87: 3.788578991  G402: 4.576638579  HCT116: 3.353065931  CRL1690: 3.282791422  AGS: 4.885228028  Panc1: 4.67900208  HMCB: 6.130147374  MG63: 5.663409796  Snu-182: 2.068010165.  Number of positive cell lines: 14.  Mean: 26.65898572.  Mean(log): 4.405086347.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>830</geneId>
<geneName>CAPZA2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>1999</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>tttttccccctcaacactgtatccccagagactaacacagtgccccgcaccccgttaaagaaccaaaaaatatttgttggatgaataaaGGAGTATATCAAGAGCAATCTTTCAATTATGGAGAGGGTCGTGATGTGTATTTTAATGAAAGCCAACTATCTTCTCTAATATTTGAAAAAACAATGTTTAAAAGGCTTCTATTTGTACACCTTTTCACATTTTAGCTGGCAGAGTTCAGGACTTGATGGAAACATAACGAAGGGCTCAGAATGTACTCATCGCAGACTGAGCCCATATGGTCACAGTGGGGAGAGCACGCTGCACTCAAGATGCTAGCAAGCCTGCAGCAGGCGGCCCAGCGAGACACGGTCCCCCGCCCGGCCACCAGGCGCCCGCGCACGCGCACAGCCGCGCTCAGTCCGCGAGGGCCGGGTCGAGGGAGGCGGGGCTCCCGGGGTGCGCGTGCGCGGCGGCCTGAGCGGCGGGCCCCTCCCTTAGCGGGGGCGCGCGGCGCTGAGGACCGCACGGAAACGGGGAAGTCAGGTGg</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003434</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: suppression of tumorigenicity 7.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.5  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.76804931  HeLa: 0.946824394  HT1080: 0.598276956  MRC5: 1.064335366  JEG3: 1.635222791  U87: 0.992085746  G402: 0.997255864  HCT116: 0.866408763  CRL1690: 0.756619734  AGS: 1.053205147  Panc1: 1.05909984  HMCB: 1.423150656  MG63: 0.818300657  Snu-182: 1.14509123.  Number of positive cell lines: 0.  Mean: 1.046811708.  Mean(log): 1.00885189.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>7982</geneId>
<geneName>ST7</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2000</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TAAATAGCATCTGCCACCCAAATCTTGCTGAATAGAGTGATTTATCTTCAGGCCTACTAGCCGGCGACAGGAGCGCACCTCCTCCCTTCTCCTAGCTGTCCCGGGTTTATTCATTCCCTGAGCCTGAATCCTGATAAGGGagcagagtagggtttaagacctcggaccccagaatacaccactgcaattgaattttggttccaccttaaggtaaactacgcagctgctgtgagcctcagtttccctacctatagaaagaggatcgtagtggggaattgttgcaggggttaaatgagattgtacggatcgtggagcagcgcctggcgtgtggtaaacgctcaacttatgcgggttgtAACTGCCTGAGGCGTTTCCTTCGGCGCGCCACTTGGCCTTCTCTTTCTAAATATTAGCATAATAAATATAAATGGACCCAGAACGCGAGGGGGCAGGGGCCACGTGATCGCTCCACGAAAGCCACTTGTAGGGACCTTTAGAGAGTTAGCAATAAGGCTGGAGAAGGA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003435</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: suppression of tumorigenicity 7.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.453703704  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.17552254  HeLa: 0.828561058  HT1080: 0.360968085  MRC5: 0.912438127  JEG3: 0.427796261  U87: 0.824405198  G402: 0.829148051  HCT116: 0.625789124  CRL1690: 1.085900526  AGS: 0.512290659  Panc1: 0.300935294  HMCB: 0.518373209  MG63: 0.491523976  Snu-182: 0.986931909.  Number of positive cell lines: 0.  Mean: 0.579190015.  Mean(log): 0.63432743.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK055405</geneId>
<geneName>AK055405</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2001</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>aattctcccaaggatggaacattctagataggagggatagaagcaaatcattctatacgttggaagcattggggcttcgtattcttgtggaaccttgttgagaagggcAGGTGTCATCCAGGAAAGAAGGGACCACAGTACTTTGCTGTGCAGCATGGGGAAAAGGGAGCATTTATGGACATCAACCAGGATGAAGCTTTCCTCCTGATTTTCAGAGGCTTCACTTTTGTGCTTTTTATCCAAGTCAGGTTAGTGCCCAAAACAAAGCAAACAAATAAAGGCCTTTATTTTAAGCCAACCTTGTAACATCTCCATTCATTCTACAGCTCAAGGTGAGGCTCCCCGAGGACCCCACATTTTAGTGTGTGTGCATCACCCAGAGTACAGACTTTGAGCGATGCCTGTTATCTAGCTGCGCTGGCTCATGTTCAGCAGTTGCAACAGCTCCATGGCTGCAATGGCTCAATATCAGCAGTTCCTTCCCCACTCAACCACAACTTCAACAGTTCTAAATCTGTTTTTGGCCAAGTCTTCAGGATA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003436</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:782833 ST7OT2 mRNA, non-coding transcript".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.411067194  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.084644735  HeLa: 0.718500467  HT1080: 0.403341314  MRC5: 1.133014951  JEG3: 0.285999295  U87: 0.47877901  G402: 0.504361568  HCT116: 0.556187488  CRL1690: 0.902010749  AGS: 0.252689773  Panc1: 0.539494748  HMCB: 0.835926311  MG63: 0.920990726  Snu-182: 0.875909281.  Number of positive cell lines: 0.  Mean: 0.553604539.  Mean(log): 0.606560744.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>93654</geneId>
<geneName>ST7OT2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2002</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GGATCTAATCAAATCCCCCAAAATGTCCCAACAAAGTATACATTTGTCATAGTCCACAAAAAGATCAAGAAGTCACTACTTAAGATAACAATGaataggtgctctctcaaatgtaacatgttcaaaactgaactcgtaattttctctcaaaaaacctctctcaccccagacttccacatcttagctgacacaaactccttccctttcaaggcaaatatttagaatcagccctgacttctcttttttcttgtactgcatatctgattaattagcaaattctgctagtcctgccttcaaaatatatctagaatctgatcacttcacaccaccttctctgctaccactctggcctgagctgccattgtggcttgccaagattaatacaagagcctgctgaccgactcctccgcttctctgctgctacacagcagcctgtaaaaattaagactggtcatgtcactcctctgttcaaaaccttgcaaagctctccatttcacccagagtaa</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003437</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: wingless-type MMTV integration site family member 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.596566524  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.176452742  HeLa: 1.005570503  HT1080: 0.653508115  MRC5: 0.358071304  JEG3: 0.426802524  U87: 1.12838215  G402: 0.476369998  HCT116: 1.030105525  CRL1690: 0.842762899  AGS: 0.501143636  Panc1: 0.653273332  HMCB: 0.698301658  MG63: 0.447780843  Snu-182: 0.715456043.  Number of positive cell lines: 0.  Mean: 0.597601582.  Mean(log): 0.650998662.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>7472</geneId>
<geneName>WNT2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2003</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GCAGCTCCAAATTTACAAGTGCTAGCTCTTCATCCCAGCTTCAGGGAGAGAAGCGAAGCAATGAGTTGAGAATCATCTCTGGATTCTTGTATCCCATGCATAGTAATCTCCTTATCCCCTGGCCCCCTTCCTCGTTTCCTCACATTGCACGCTCAGGGACTTGTTTGCCAGCGGATGGCCTCGGCAATCCGGAACGCACGCTCCGAGAGCCCACGGATGCTCTTTGGCCTGGAGCTTCCCTAAAGGTTCCTGTATTCGCGTGTGCTCGTAACCATGCAGCGATGTTCCCCCTTCCCCGCCTCACCTCATCCCCAGACATCTCTTGCCATCATTTCATGCACCCGTGTCTAAAACCCCGCGTTTCTCCCCACCCCCGCCAGGCGCAGCACCCCCTCCCTCGGCTGCGCCCGGAGGGGAGCAGAGCGGACGGGGCGCGCGGGAGGCGCGCAGAGCTTTCGGGCTGCAG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003438</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: GASZ.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.613686534  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 3.812587023  HeLa: 2.956919142  HT1080: 2.960026902  MRC5: 1.505322929  JEG3: 3.886560891  U87: 3.544352397  G402: 2.376899823  HCT116: 1.831696783  CRL1690: 4.847127819  AGS: 2.881226735  Panc1: 1.827876847  HMCB: 3.735752565  MG63: 3.308321587  Snu-182: 2.527363487.  Number of positive cell lines: 11.  Mean: 8.738610408.  Mean(log): 3.000145352.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>136991</geneId>
<geneName>ASZ1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2004</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTGCCGTTAAATCCTAGTGTGCTCCTGCCACAAGTAAGGCATTCCTTGCAGAGCAAGAATTTCATCATTTCATCAAGCAAATACTTTAAAGAGGTCGAAAGGTAAGTCCCTGAGAGGAACTGGAAGTGCCAGCAGAAGCCTGGCGCACGAACTTCGTCACCAGTGTCAGACACGCCAGGTTTTCACCTCAAGAAGCCTCAAGGTTAGGGAGGGACGGGGCAGGGAGGAGAGCAGCGCGCCGCTGTGCGCCTGCGCTGGAGGGCTCCAGACTGGAGCGCTTCCACGGCGCTCCTTCCCGCGCATCTCTACGTACGCCCCACCCCGGTGCGCATGCGCCCGGAGAGCTGAAGGGCGCGCGGTGCCGACAGGGAGCTTCCTTGGCTGGCATGGCGGCGAGCGCGCTGCGAGGCCTGCCAGTGGCTGGCGGAGGCGAGAGTAGCGAGAGCGAGGATG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003439</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: testis derived transcript (3 LIM domains).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.408536585  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.36228178  HeLa: 1.00078111  HT1080: 0.821637382  MRC5: 1.149873629  JEG3: 0.841161064  U87: 2.106949969  G402: 0.855003593  HCT116: 1.142790133  CRL1690: 2.326104189  AGS: 0.719609008  Panc1: 1.007020504  HMCB: 0.712255869  MG63: 0.809303814  Snu-182: 1.038084222.  Number of positive cell lines: 2.  Mean: 1.25030269.  Mean(log): 1.063775448.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>26136</geneId>
<geneName>TES</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2005</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AATCTACTCATCCCCTCACCCATGTATTATGATGGGTTACCCCTGAAGAAATAATACCATAGCCTTTAGGCATCGCAAGAATGATCGCAGTATTCAAGTTTGGGGATAAAGAGCCTTAATTAAGACCTCTCAAAGCAGCTCTCTGTGGGATCCACCCTTTAGAAGCAGCTGTGGAGATAGTGACACAAGACCAAATTAGGAATGGTTGCCATGATCCAGATTCTTTTATGGAACTCCTACAGATGCGTTTTGGAATCAGGTTTTTAAAGTCCCTTTTATAGCAAATAAATAGGAGGTTTTGAGGGCTGTTTATGAGCGCATTCCATTACAGTGTCTTTCAGCGGAGCCAGAGCTCAGCCAATCCTAATTAAGAAGCAATTTCAGCTGCAGTCATTGCTTATTATAATAATTGTGACATTTTTATAGCCCTACATTGTCTTTCTCAAAGTAACGGATTCAGGAGGAGTCCTTTTCTGAGTAGAGTCCACAGAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003440</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: testis derived transcript (3 LIM domains).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.617760618  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 5.394805881  HeLa: 3.363369664  HT1080: 3.195598323  MRC5: 1.669832587  JEG3: 4.458263232  U87: 1.649508639  G402: 3.417623014  HCT116: 3.509062471  CRL1690: 2.081854237  AGS: 5.060350231  Panc1: 3.74699469  HMCB: 2.218391601  MG63: 4.673849557  Snu-182: 1.876233017.  Number of positive cell lines: 11.  Mean: 13.05532074.  Mean(log): 3.308266939.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>26136</geneId>
<geneName>TES</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2006</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AGGAATCCCTAACGATCCCTACAATCTCTCTCTCTCTCTTTTTTTTCTCTCTTTACCCTGAAAATAAACTGAGAAGTTAGTATTGGGATAACTATTCCCCTTGACCCAAATAAAAAGTCCTGGGCAAACACAGGTACAAATTGCCAAATGGAAAAAGTTCTTCTCCATCTTCAGCTAGAGGGAGGCTGGGGATCCCAGCTCTTTAGAAGCCGGCCCGTGGACGCCCAGAGAATCCCTTCGGAGACCAGGTCAGGGTCACTGAGCTTGCCCAGCAGGGCGCCGCCTCGGACGCCGCCCCGCCTCTCACCTTGCCAGCGCCGCGCTCGGGCCGCGAAGGTGCGTGCGGCGCTCGGTGATTGGCGGCGGCCCGGAGCTGCCCGGCTGCCATTGGCTGCCCGGCCCCCTTTGTTCCCGGGTCCGGGCCGCAGGCCCGCTGCGGCGGACTGGGCGGCGGAAGTTCGACGGCGCCGGGCGAGTGGCTGTTGAGCGGCGCCGCGGGAGTTCCGCAGGTTTCCCGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003441</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: cortactin binding protein 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.351145038  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.788537824  HeLa: 0.963095526  HT1080: 0.491360752  MRC5: 1.059020403  JEG3: 1.184157265  U87: 0.720678186  G402: 1.000980861  HCT116: 0.718020558  CRL1690: 1.007105922  AGS: 0.615915883  Panc1: 0.632983238  HMCB: 0.69616979  MG63: 0.664024637  Snu-182: 0.648932627.  Number of positive cell lines: 0.  Mean: 0.757037178.  Mean(log): 0.799355962.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>83992</geneId>
<geneName>CTTNBP2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2007</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>tgtgggtgctgacactcagtaattttttattcttctttATATATACCAAAATTTCCATAATGAAATGCATTACTGTTTTAACCACGAACAAGCTAAATAAGCATTGACAAAATTCCACATAAAGAGCATCTGCAAAGGATAATATAGAAAAAGTTACAGAATTTCTGGAAGGGACAAAATGAACTTGGAACTGTGTGTCTCAGCTACCCTGCAGACCCTCGCTATGGAAAATAGAGGGAAAAAATGTGTTTTTTTATAAAGTATCAGCTCTTGCTAAGTACCCTTTGCCCATGTTTCACATTCAAATGAGAGTACAGGTGTCCAATGATAAAGCTAATCTCTAAAATATTGTTTTTAATCTTTTGAAAGTATGAGGACAATCAAAAAAGAATTCCACACCTGTGTACCACTTTTTTCTCTCATCAATTTAGCATCTTCACCCTAGCTCTCTACTTGGTTTGTTAATAGGTTGAGCAATATCATAATGTCATTTTCCACGGCCCAGAAGGAAGCTTGCAAGACTA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003442</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.38021978  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.563326462  HeLa: 1.321707045  HT1080: 0.652596387  MRC5: 1.205772084  JEG3: 0.903248308  U87: 1.130217286  G402: 0.713627071  HCT116: 1.172210121  CRL1690: 2.496230518  AGS: 1.101603316  Panc1: 0.792379045  HMCB: 1.405392542  MG63: 1.275577992  Snu-182: 1.095959706.  Number of positive cell lines: 1.  Mean: 1.323994944.  Mean(log): 1.13070342.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK097428</geneId>
<geneName>AK097428</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2008</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ccctctagagaaccctggctaaACActtatttcatttttgtctataacacttatacaacctggcttatataaatctgttttgttattcattcattgttgtcacgtcaacaatagtaatattcatagttcaggcacattgtgtattttgttcactgctgtaaaactaaaatgatacttggcacagagttgacactcagaaatatgtgttgaataagtaaatTCTGGTGTGGCATAGAGTTCTGGCTGTGGTCCCATCCTGCAGAAGCAAAATTCTTTTAGTATTGTGAGGTCACAGAGTCATGGCATTCTCACTCGCATCTTCCATGGGGAGACAGGTGGAATGGTGAGGTACCCTTGGAAGGTTAAGAGAAAAATTTAGTAAACACTTTTGAGTATATAGACTCTTGCTGCATGATCCCACTGTGTAAGAATTTGCTTATTTCCAGGGCTTCATA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003443</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: caveolin 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.509090909  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.412411551  HeLa: 0.558865959  HT1080: 0.40680367  MRC5: 0.781259636  JEG3: 0.577182937  U87: 0.688469893  G402: 0.549719551  HCT116: 0.860112502  CRL1690: 0.509803094  AGS: 0.91770813  Panc1: 0.649428017  HMCB: 0.573912567  MG63: 0.404770966  Snu-182: 0.782493741.  Number of positive cell lines: 0.  Mean: 0.546066596.  Mean(log): 0.619495872.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>858</geneId>
<geneName>CAV2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2009</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>aactctgccacacacacacaaacacacacacacacacacacacggtgtagtttaggaagtaaaaaaaaaaaaaaaaaaaaaaTCAGATCTCCCCTCACACCTCAGATCTGAAGGCACAAACTCTAGGGCCAGGGCGTTCGCCTACCCAACTCCACATGCACTTGCAGGTCACCTAGCACTCAGGTACCTAGCACTCAGGTACATTGTGGCTCCTTACCTCTCACGACAGCAGCAACAACGTTGATTGGAAGTTTATCACTGTGTGTTACGGGccatgggccatgtgtgttagaattttatgtgaaattaacatttaattctcacggacacccctgaaacagatgccacagcccccattttgccaacgaggcagctgaggttcccagaggctcaataccagcaccatgagccgcagcacgcaaggcaaacacagccggaggtgagcacatacctgcttcgcaccccatgcGCCTAACCACAAGGTTCCCTCCCTCCAGGAAGGCCGTTGTCTTCCCTGGGACGACTTGCCAGCTCTGAGGCATGACAGTAC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003444</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "caveolin 1, caveolae protein, 22kDa".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.539784946  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.433380028  HeLa: 2.954213628  HT1080: 3.953471804  MRC5: 2.399875539  JEG3: 1.708151981  U87: 5.122469863  G402: 4.18650762  HCT116: 3.175008529  CRL1690: 2.425563905  AGS: 3.095620199  Panc1: 2.156807563  HMCB: 1.668060727  MG63: 2.832016555  Snu-182: 0.928005036.  Number of positive cell lines: 9.  Mean: 8.081722361.  Mean(log): 2.717082356.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>857</geneId>
<geneName>CAV1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2010</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CTTAAGTTTCCATCCACACCGACTAGATGTAAACGAGTGTCACCAAAAGTACACCACAGGCACCCACACAGATTCCTTCCATAAGGGATCCACAAAGTTTAGATGTGAAATGTACCTAAAGGTTCCTAGCCGTCTTTCATCCCTCCCTCTGTGAAACAGGGAGACACATGTGTTTTAAGGCAGAGATGGAACTTGGGCGATGGGCGGGGGGTGGGGGAGGTGGGAAGGGACGGCTTAGGACAGGGCAGGATTGTGGATTGTTTCTGCCGCCTTGGTTGCCCATACTGGGCATCTCTGCAGGCGCGTCGGCTCCCTCCACCCCTGCTGAGATGATGCACTGCGAAAACATTCGCTCTCCCCGGGACGCCTCTCGGTGGTTCAGAGCAGGGAAAATGTTGCCTCAGGTTTAAAATAATCTGCCCAAGCACCCCAGCGCGGGAGAAACGTTCTCACTCGCTCTCTGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003445</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: met proto-oncogene (hepatocyte growth factor receptor).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.375  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 3.336965463  HeLa: 1.16273559  HT1080: 2.314718707  MRC5: 1.685257173  JEG3: 3.127069988  U87: 1.501889375  G402: 2.49405368  HCT116: 2.719299919  CRL1690: 0.596462109  AGS: 2.845981165  Panc1: 1.901040932  HMCB: 1.993643818  MG63: 1.092080871  Snu-182: 1.264083099.  Number of positive cell lines: 6.  Mean: 3.662516876.  Mean(log): 2.002520135.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>4233</geneId>
<geneName>MET</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2011</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTGGGAGGCTTTCTTCTTCTTTTACAAGTAATGTAAAATTGTAGTGAAGCTATTGGAAAAGAAAAGGATAGAAACATGTTAGTGCTTTGACACAGCGGGAGAGAATTTTGGAAGAGATATTCTACCAACTACAGATGGAATCTTCATCATCATGTAGACTTCAGATATTCTTTTAGAAAACTTTACATTTACTTATAATCTAAACCTTACTTGTTTAAACAAGTCATGAAATGTATAGCTTAATAATTGCCTTTAAGAAAATTGTTGCCCAAAACAGAAACCGTATTGAGTATGTAAAGCCAAGTTTAGTTACCAAGACCTACTGATTTCCTTTCATATATGTATGGTCACATCTCTCACCTCATCTGTCCTGTTTCTTGTTTTACTAGTGGTCCTTTGGCGTGCTCCTCTGGGAGCTGATGACAAGAGGAGCCCCACCTTATCCTGACGTAAACACCTTTGATATAACTGTTTACTTGTTGCAAGGGAGAAGACTCCTACAACCCGAATACTGCCCAGACCCCTTGTAAGTAGTC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003446</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: met proto-oncogene (hepatocyte growth factor receptor).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.352422907  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.133449275  HeLa: 0.874347117  HT1080: 0.375004542  MRC5: 0.683709303  JEG3: 0.52666674  U87: 0.912792529  G402: 0.943548131  HCT116: Bad Txfn  CRL1690: 0.745237091  AGS: Bad Txfn  Panc1: 0.256343171  HMCB: 0.484529722  MG63: 0.342691919  Snu-182: 0.931024442.  Number of positive cell lines: 0.  Mean: 0.543692631.  Mean(log): 0.600778665.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>4233</geneId>
<geneName>MET</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2012</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AAAAACCCACTGTTTGAGAATGATGCTACTCTGATCTAATGAATGTGAACATGTAGATGTTTTGTGTGTATTTTTTTAAATGAAAACTCAAAATAAGACAAGTAATTTGTTGATAAATATTTTTAAAGATAACTCAGCATGTTTGTAAAGCAGGATACATTTTACTAAAAGGTTCATTGGTTCCAATCACAGCTCATAGGTAGAGCAAAGAAAGGGTGGATGGATTGAAAAGATTAGCCTCTGTCTCGGTGGCAGGTTCCCACCTCGCAAGCAATTGGAAACAAAACTTTTGGGGAGTTTTATTTTGCATTAGGGTGTGTTTTATGTTAAGCAAAACATACTTTAGAAACAAATGAAAAAGGCAATTGAAAATCCCAGCTATTTCACCTAGATGGAATAGCCACCCTGAGCAGAACTTTGTGATGCTTCATTCTGTGGAATTTTGTGCTTGCTA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003447</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: acyl-CoA synthetase long-chain family member 6.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.454365079  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.476725101  HeLa: 1.100931399  HT1080: 0.471687016  MRC5: 0.99507231  JEG3: 1.281773178  U87: 1.798893518  G402: 0.811240053  HCT116: 1.201988783  CRL1690: 0.562981649  AGS: 0.806520685  Panc1: 0.572094644  HMCB: 0.651177289  MG63: 0.625258678  Snu-182: 0.973998086.  Number of positive cell lines: 0.  Mean: 0.905201291.  Mean(log): 0.880738742.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK122702</geneId>
<geneName>AK122702</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2013</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTGCAGAAGTGCTTTACCATTCAAGCTCTGTGCAGTACAGCTCCGTTTATGACCAAAACACTTATGTTCCATAACTTTTATAATTCACAAACTCCTAAAAGAGAAAACAAAAGAGTAAAGTTGGGGAATGAAACTGGCATGGCTCTTCAGGCTGCAGATGGGGACTGGCCTGAGGCTGGCCCTGAGACAGGCCTTGTGGAAGTACAGAGGGAGTGGGAGGAGGAATCCATATGTGATTATGGAGACAAGGAATTCTCCATATATGTGTCACTCAAGGGACCAGCATATGAAAAAACTGTGTCTTCTAGGCCTTTCCCATTTTGCCTTGGGGGAGGTCTTATGTAATAGTgcaggtaaggccgtggcatctggagagcatgctttccagctttccagacctggattcaatgccagcaattactgtaaattagttttgtgaccctgggcaagtcatgtaacctctctgagctttgtgttccttacctgtagaaatgccacttccct</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003448</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: acyl-CoA synthetase long-chain family member 6.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.597042514  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.334269119  HeLa: 0.90724889  HT1080: 0.328175165  MRC5: 0.995055505  JEG3: 0.375245461  U87: 0.718533933  G402: 0.716504834  HCT116: 0.780587711  CRL1690: 0.822505433  AGS: 0.600955565  Panc1: 1.243402107  HMCB: 0.799319171  MG63: 0.661561477  Snu-182: 0.940678262.  Number of positive cell lines: 0.  Mean: 0.684474495.  Mean(log): 0.73028876.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>23305</geneId>
<geneName>ACSL6</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2014</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGCCACATACAGTTGTGTACGAAGATCATGATTTCCTCATGAGACACCTGTGATTCCATGTGGCTGCCTGTGACCATGTTACTACTGGTGAACACATATGGCAGCCTGTGATCACACTGAGTCTCCTGTGACCTTGCGTAGCCTCAGACCTGAACTCGTGCGTCCCCAGATGATCTGGGCACTATCTGGTCTAGCTGCCTGATTTGTCAGAGCCTAGGTGAACACTTGCCACTCCCTCCCCTCACTGGTTTGCAGAGGTGGCACCCGGAGGCTCCCCATGTCTGCAAACTCGGGTCCTAGGGGGCGTTGGTGTCAGCGGGCAACAGCCCACAGGAGTGTGCACCTCCTAGGACAGGTAACCGCGACCCGGCTGCCATTCGAGCCTGCCCAGCCATAAAACCCAGGCTGCGAGTCGCGCGGGGGCAGGGTCGCGTGTTGATGGGGTGGGTGGCGGCGGGGTGGGCTCAATGTCACGCTCTGGCGCTCGTCGCCCGTGCTCCCCCTTCCAGCCGGTTTCCGCAGAATGCCAGGTACTGACGTT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003449</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "solute carrier family 22 (organic cation transporter), member 4".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.712273642  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 5.085358285  HeLa: 3.891436073  HT1080: 4.426644737  MRC5: 3.082627743  JEG3: 4.23881512  U87: 3.57631529  G402: 4.61657637  HCT116: 3.765953624  CRL1690: 3.05130134  AGS: 3.925342202  Panc1: 4.264035517  HMCB: 3.411019716  MG63: 4.03187061  Snu-182: 1.658403766.  Number of positive cell lines: 14.  Mean: 14.75423024.  Mean(log): 3.787550028.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6583</geneId>
<geneName>SLC22A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2015</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CCTAAGCTCAGCCTCCAGATTGGAGGAGACCGCGGAGGGAACCCTGCTGGGGTCTGGGCCCGGGGCCACGCGGCCCGAGCAGATCGAGGGCCGACCCCTCCGAGAACTCGCTCTCTGGCCTCGGCTCCTCCCTTGCGCCCGCCCTCCCACGTGGGGCCCAGGTCTGGGAATCAGCGCTCGGGGGTGGCTGGGGACAACCGAGAACGAGCTTCTTCCCCGGCACGCGGGCGGAATGGCTGAGCCCAGCCTGGAAGCCCCCGTCAGGTCCTTGGGGGCGGGCGGGCGCGCGAAGCACAGGGCGGAGACAGCCGGGAGCCCAGCCTCCCGGGCTGGGCCGCCCTCCCCTTCCCCGCGCCCGGCCGGGGATGGGGGTGTGGTCCCAAGTGTACAGTGGCATCAAGCTCAGCGCGAGCTCCCGGGAACGCTCCAACGCCTTCAGCCTGTTTCCCAGGAACGGTCCCCGGCTTCGCGCCCCAATTTCTAACAGCCTGCCTGTC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003450</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "solute carrier family 22 (organic cation transporter), member 4".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.709923664  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 4.100779431  HeLa: 2.760463277  HT1080: 3.019162523  MRC5: 1.719923633  JEG3: 0.733292849  U87: 1.417154396  G402: 3.09673145  HCT116: 3.323494991  CRL1690: 1.137979419  AGS: 3.42592602  Panc1: 3.345376846  HMCB: 2.341139135  MG63: 2.755365062  Snu-182: 1.112723599.  Number of positive cell lines: 10.  Mean: 5.809104376.  Mean(log): 2.449250902.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC043424</geneId>
<geneName>BC043424</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2016</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GTGGACAGGTAGACGTCCTGACTGAACTCCCAGCCATCCAGACAGCTCTCCTGCTCCAGCTGCCCCAGGTCCACGTCGCGCCCCGGCTCCAGCCCAAGCGCCGAGAAGTTGGCGATGGTGGCGAGCCGGTAGCGGCGGCAGCTGTGGGGCACCTCGCGGCCGTCCCGCAGCCGCAGTGGGACAGTGTGGTTGCGCCAGGCGCTGCTCAGGTTCGCGGCGTCCGGCACCCGGCAGCGGTGCTCCGGGGTCGCTATCAGGAACACGGAGGACAGGCCGGTGAAGCCATTGGGGATGATGCTGGCGCTGAGCAGGAAGAAGATGAGGCGCTGGAAGGGCCCCCACTCGCCCAGGAAGGCGGTCACCTCGTCGTAGTCCCGCATGCCGCCCTCAGAGGCCCACAGAGCGCGGCCTGGGGTCGGGGAACGCGGCGGGCTTTGCGCGTGCGCGCGGGGCACCCGCCGCCGACCAGGCAAGCCAGGCAGCAGGCGACCCAAGACCGTCCGCGGAGGGTAGGCTCGCGAGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003451</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "CDNA FLJ44796 fis, clone BRACE3040504".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.45540797  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.093677049  HeLa: 0.562436438  HT1080: 0.587781431  MRC5: 1.190332393  JEG3: 0.451439033  U87: 0.978737257  G402: 0.362890967  HCT116: 0.549983997  CRL1690: Bad Txfn  AGS: 0.362587009  Panc1: 0.599495778  HMCB: 0.658288035  MG63: 0.317591141  Snu-182: 1.045744896.  Number of positive cell lines: 0.  Mean: 0.546680954.  Mean(log): 0.596998879.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK126749</geneId>
<geneName>AK126749</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2017</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>tagccgactgacacctcatacaggcaggtgcccctctgggatgaagcttccagaggaaggatcactcagcaatatttgctgttctgcaatatttgctgttctgcagcctctgatggtgatacccaggcaaacaggtctggagtagacctccagcaaactccaacagacctgcagctgagggacctcactggtagaaggaaaactaacaaacagaaagaaatagcatcaacatcaacaaaaaggacatccacaccaaaaccccatctgtaagttaccaacatcaaagaccaaaggtagataaaaccacaaagatggggagaaaccagagcagaaaagctgaaaattctaaaaaccagagcacctcttctcctccaaaggatcacaactccttgccagcaatggaacaaagctgggtggagaatgactttgacgagctgacagaagtggacttcagaaggtcagtaataataaacttctcccagctaaaggaggatgttctaacccatcgcaaggaagctaaaaacctt</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003452</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:4795753, mRNA".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.489035088  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.545778307  HeLa: 1.116764849  HT1080: 1.383328644  MRC5: 1.166219679  JEG3: 1.238583761  U87: 1.283338952  G402: 1.597090542  HCT116: 2.494478362  CRL1690: 1.582457991  AGS: 1.672156301  Panc1: 1.736915889  HMCB: 1.488745305  MG63: 1.189505418  Snu-182: 1.130850708.  Number of positive cell lines: 1.  Mean: 1.870527757.  Mean(log): 1.473301051.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC033946</geneId>
<geneName>BC033946</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2018</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>atgatcctggaagacaagagctgagcaggctctcagcattctccttgcttcccactgccatttctaaatcataactccttcaccttcacatacataaaagacctgctcaggtttgtgctgtgccctcctggttgctgttaccaacatctgcctggttggttatccacattctgtgagctctctgacacccagcccaaggtgctggtgacttttgtgctcaggaagatgagtagtgctacaccttagcctcgcagtacttgaccttcacctatacttcacactcttgctgctgaggacacaccctgggcctctcatcagtcacaacagctccatctcactctaggacctttgttttcctcccaactcttcagctctcacctgatatcatttcctttccctttcagtttataccttGTGATCCCTCCAGCCCATTCATACTCTTGCCACTACCCCAGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003453</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "solute carrier family 22 (organic cation transporter), member 5".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.490384615  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.916832281  HeLa: 1.186406346  HT1080: 1.209145945  MRC5: 0.949371031  JEG3: 0.857427083  U87: 3.918546065  G402: 1.185613187  HCT116: 1.362097997  CRL1690: 1.020461186  AGS: 0.781099455  Panc1: 0.622798052  HMCB: 1.030710506  MG63: 1.047671956  Snu-182: 1.173103017.  Number of positive cell lines: 1.  Mean: 1.988397949.  Mean(log): 1.232948865.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6584</geneId>
<geneName>SLC22A5</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2019</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ACCACACAGCCAGGTACTCTCTCTGACCCAGAGGGCAGGGAGCCAGGCTTCGGGAGGAATACTTAGAGGCCTCCTTGGAATGTGGCCACCGACAGGAATATGTGGGGGTGCAGTGAGGAAGCTGTCAGCCTGGGCCTCTGTCTTCCTGTACCCTTGAGGGACTGGTCACTTACTTTTCCTCATTTTCATTCACTCTGATTTGTTACTGACAAGGCCTAGGGAAGTTTTCACAGCCTAAAACACAGTCAGTATACTTACTGTTCTTAGAAACGTAACACTCCCCGACGCTGAGATGCAGACAGCTAAGATGCCAGGGATTCAAGTATGTTATTGTGTGCTCTGAGTCTCTGACCACCTCTTCTTCCCATACACTTATGATGTTGTTCCTGCAGTTACAAGACCTAAGTTCCAAGAAGCAGCAGTCCCACAACATTCTGGATCTGCTTCGAACCTGGAATATCCGGATGGTCACCATCATGTCCATAATGCTGTGGTATGTAAAAGAGACCTGCCTGAGGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003454</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "solute carrier family 22 (organic cation transporter), member 5".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.666666667  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 4.616696842  HeLa: 2.971722939  HT1080: 2.923859155  MRC5: 1.272095364  JEG3: 2.59102608  U87: 1.9970741  G402: 2.680009262  HCT116: 4.077135007  CRL1690: 2.235304525  AGS: 4.751995761  Panc1: 3.489534461  HMCB: 2.897894789  MG63: 2.525386593  Snu-182: 1.269053009.  Number of positive cell lines: 11.  Mean: 8.585287845.  Mean(log): 2.878484849.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6584</geneId>
<geneName>SLC22A5</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2020</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AAGTCATAGCTCCCAGCCTCTCTACTAGGGTAGTTAACAGTCCCAGGTTCAAAATAATCCCCGTCCCTCTTATAAGATTAGGCGGTGTCAAGAGCAACTATCTGTGAGACCCTGGGCCAGTGACTTTCTCCTTACCTCCGCCCCCAAGTAGGCCTTGCAAAAAGCTGGGAGGGGTGCGTTTTCAACACTGGAGCTTCGCGGCCGCTCTCCCACTCGCTCCCCGCCCGGCGCTAGAGGAGCGAGTTCGGACTCGGACCCCAAGGCCTCGAGTCCCGCTGCCTTCCTAAGCCGAGCCCGGGCTACCTCGGTCGTCCCCAGCAGGCTTGGCTGGCAGAGGCCGGGCCTCGCCAGGTCCCCAGGACAGGCCCCGCCCGGGCCTCAGGTGCACTcccggcccgccccgcgccctcgcgtcccgccccagctccgccttcgccggcgccgctctgccTGCCAGCGGGGCGCGCCTTGCGGCCCAGGCCCGCAACCTTCCCTGGTCGTGCGCCCTATGTAAGG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003455</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "CDNA FLJ46914 fis, clone SPLEN2027852".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.524680073  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.671444775  HeLa: 1.03359527  HT1080: 0.48841119  MRC5: 1.039241222  JEG3: 0.312245342  U87: 0.932750448  G402: 0.45830389  HCT116: 0.663869398  CRL1690: 0.337024061  AGS: 0.760400091  Panc1: 0.701009631  HMCB: 0.805161397  MG63: 0.281878799  Snu-182: 1.142601312.  Number of positive cell lines: 0.  Mean: 0.981306593.  Mean(log): 0.830566916.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AF086145</geneId>
<geneName>AF086145</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2021</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CTTCTCTGACCAGTGACAGCCCTCACAGGCAAAGCCTCACCCTCTAGGGCCTGTCCCTTCCTGTCTGCCAGTCCCCACAGGGTCTGCGGGGTACCCAATCTCGCCAACCAGACTGGAAGCTCCCCAGGGGCAAGCAGCTTATCTCTTCCATATTCTCACAGTGTTCAGCCAGGATTGGCACTTCAGAGCATCTCCTGCTGCTCAGCAGAGATGTAGTTAGCATCTCTCTATAGTAGCACTTTCTGAGTCCCTCCCCTGGGGGAACCAGGCTAGACTCTGGGGTCCAGAGGAGCAGGCAGGCTGAGAGGCAAAAAGGGCACAGAGGAATAACCAACCCTGCCCCTGCAGTAGAGCCCTGGGCAAAACAGGCCATGACCAACCAGCAGCCAAGGTCAAAGTCCCCAGAACAAGGGCCAGTGTGTGCATGACATGCAGCATGACCGCTTGTCTCTTTTCGGCAGTACTGGAGATAGAAGGCTGAGTCATTAACAACTTTCTTTTATTAAAAATGTACATAAGTAAAAGGAACATGGTTTAATTGTGCAAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003456</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "CDNA FLJ46914 fis, clone SPLEN2027852".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.496062992  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.21416765  HeLa: 1.219107168  HT1080: Bad Txfn  MRC5: 1.039194903  JEG3: 0.353031077  U87: 0.655252643  G402: 0.689065749  HCT116: 0.708263328  CRL1690: Bad Txfn  AGS: 0.81259141  Panc1: 0.700270117  HMCB: 0.649725402  MG63: Bad Txfn  Snu-182: 0.980136696.  Number of positive cell lines: 0.  Mean: 0.68764032.  Mean(log): 0.729164195.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK025221</geneId>
<geneName>AK025221</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2022</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ttagtagagtcggggtttcaccatgttggccaagctggtctcgaacttctgatctcaagtaatccaccctcctcatcctcctaaagtgctgggattacaggcatgagccaccgcgcctggccCCATTTGAtttttttaagagacagggtatcacttcatcgcccagactggagtacagtggtgtgaccatagctcactgcagcctcaaactcctgggctcaagtgatcctcccacctcagcctcctgagtagctgagactccaggtacacaccaccacacccagccaattttttttttaagacagggtcttgctatgttgcccaggctggtcttgaacttctggactctaatgatcctcctgccttggcctaccaaagtgctggaattataggcgtgagccactgcacctggccCCATTTGATTTCTAGACTAGCATTTTAGTGGTGCTTCAGGAGAGAAAGGAAACTAGGAGTGTAAATAACTGATGTGTTGAACTGGAAACCCTGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003457</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:5745162, mRNA".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.546845124  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.500168505  HeLa: 1.259613855  HT1080: 2.202079733  MRC5: 1.730617379  JEG3: 0.442160374  U87: 1.493189184  G402: 2.14912853  HCT116: 1.059215006  CRL1690: 1.213710329  AGS: 2.464468828  Panc1: 1.950377853  HMCB: 2.352520202  MG63: 1.804866073  Snu-182: 1.07097284.  Number of positive cell lines: 3.  Mean: 2.505027904.  Mean(log): 1.692363478.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC044238</geneId>
<geneName>BC044238</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2023</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CTTGGTTAAGGGCACATTTTCTGGCAAATTTGGTAAATAGCTGAATATTCTGGCATCCCCATAGTCTGACAAAATTCCTCTTCTGAATGCCTCAAGAAGAAACAAATCTGAATTTCCTCCAGTTTAGCAAAAGGCTGTGCTGGTCAACGGGAATCTGCCACCTCCTGAATCCCCCCTCTGGAGGTCAGGCGGCACAGCAGCTGCAGCCTTAAGCTGCTCTCCCTCCGGCAGCAAGCGGTCAAGTTCTGCTGTTGGCCTGTGAGAGCCTACAGTGTCCACAGAGTTAACATTAGACTGGAGCGGCCCAGCCCTCAGCGGGCAGGAGCACTGGGAACTCAGGCCTCCTTTTCAAGGCCAGGATGAATGGGAAATATGCAAATGGCCGCCTCCCAGGAGCGGCAGGGGAGGGCCTGCTGCTGGCAGGAGGGCATCACTCCACTTGGGTCTGTCACATGAAAGGGTTTGTATTCCTGCCGCTGGCCGGCTCCTGGCCAGGCTGGGGCTGTTCTCACCAGAAAACAAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003458</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: MRNA; cDNA DKFZp686D10250 (from clone DKFZp686D10250).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.521317829  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.099091881  HeLa: 1.265239616  HT1080: 0.273808983  MRC5: 0.983465587  JEG3: 0.287283354  U87: 0.764576441  G402: 0.627740701  HCT116: 0.562031758  CRL1690: 0.196303225  AGS: 0.295672006  Panc1: 0.355230636  HMCB: 0.500000196  MG63: 0.58372746  Snu-182: 1.096368936.  Number of positive cell lines: 0.  Mean: 0.521797931.  Mean(log): 0.563610056.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AL713721</geneId>
<geneName>AL713721</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2024</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ATGAATCTTCTCTAGCCCCGAACAGCACAGTGAATGGATAGGGCAGCAGATGAGCTCTGCCCCACGCCGGCCCTGTTTCAGAACAGCACTCCAGAGTGCCGCACTGCTTGCTGAACCACAGCTGTTACTGCAGATTGAGGAGCCTCAGAGGGAACAGAAGATAAAGATCATTATGGAATTTAGGATTGCAGGACATTCTTTGACATTTCATAACAGCCAGGGGAGATCAACTGTGGTCAGGGGACAGGGGCAGGAAGAAACCATGGCCAAGGCCTGTCTGGCAGGACTTGAAGGGGCAGAGGGACCCTTGCAAATGACCCTGCCTGGAACCCACCCCCAGTTGGCCCCTGTATAGCACTGATCCAGCTGGGGCTTTTATCCCAGGATACCCTCTTCAGGGATGCCTGTATTTGTTGATTATCTGCCATATGCCTGGTCACTGCAGAATACAAGGAAGAAAATAGCCTTCAGCAGAAGCTGAGACAGGAGCCTAGAGGATGGACAGTAAGGAGTCGA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003459</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: interferon regulatory factor 1.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.73271028  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 8.506092937  HeLa: 7.445610598  HT1080: 7.571415752  MRC5: 6.26430447  JEG3: 6.643954136  U87: 7.781392056  G402: 6.275061875  HCT116: 6.281352312  CRL1690: 6.170393215  AGS: 7.505453689  Panc1: 6.214931291  HMCB: 7.154058206  MG63: 8.476641995  Snu-182: 4.479567493.  Number of positive cell lines: 14.  Mean: 151.0835964.  Mean(log): 6.912159288.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3659</geneId>
<geneName>IRF1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2025</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CACCTGCGTTCGGGAGATATACCCCCGCCCCCGCCCCGCCAGGAGGGTGAAAAGATGGCCCCAGGAGCCAGCCGGCTGGGACAAGGCGGAGTGAGAGGACAGGCTGGGGCCAGGGGCGCTGGGCTGTCCCGGGCAGCCCTCCTCCGGGCAAGCCGGAGCAGGGGTGGATTGGGAGCGCTcggggcgggcccgcggtggccccggggcggtggcgcccggccggAGAGGGTGGGGCGGAGCAGCCGCCCTGTACTTCCCCTTCGCCGCTAGCTCTACAACAGCCTGATTTCCCCGAAATGACGGCACGCAGCCGGCCAATgggcgcccgcgcggctgtccgggggcggggccggccAGGGCTGGGGAATCCCGCTAAGTGTTTGGATTGCTCGGTGGCGCCGCTGCCCTGGCAGAGCTCGCCACTCCTTAGTCGAGGCAAGACGTGCGCCCGAGCCCCGCCGAACCGAGGCCACCCGGAGCCGTGCCCAGTCCACGCCGGCCGTGCCCGGCGGCCTTAAGAACCCGGCAACCTCTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003460</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.410351201  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate>26-Apr-2007</deprecatedByDate>
<deprecatedByStableId>OREG0003045</deprecatedByStableId>
<deprecatedByUser>bcb</deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.25330029  HeLa: 0.453702419  HT1080: Bad Txfn  MRC5: 1.115239321  JEG3: 0.490537929  U87: 0.63539898  G402: 0.549378103  HCT116: 1.02280565  CRL1690: Bad Txfn  AGS: 0.299301197  Panc1: 0.974953918  HMCB: 0.362046978  MG63: Bad Txfn  Snu-182: 0.933127384.  Number of positive cell lines: 0.  Mean: 0.59747574.  Mean(log): 0.644526561.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AL137501</geneId>
<geneName>AL137501</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2026</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>tctcacaccagttagaatggcaatcattaaaaagtcaggaaacaacaggtgctggagaggatgtggagaaataggaacacttttacactgttggtgggactgtaaactagttcaaccattgtggaagtcagtgtggcgattcctcagggatctagaactagaaataccatttgacccagccatcccattactgggtatatacccaaatgactataaatcatgctgctataaagacacatgcacacgtatgtttattgcggcattattcacaatagcaaagacttggaaccaacccaaatgtccaacaacgatagactggattaagaaaatgtggcacatatacaccatggaatactatgcagccataaaaaatgatgagttcgtgtcctttgtagggacatggatgaaattggaaaccatcattctcagtaaactatcgcaagaacaaaaaaccaaacaccgcatattctcactcataggtgggaattgaacaatgagatcacatggacacaggaaggggaatatcacactctggggactg</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003461</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "interleukin 5 (colony-stimulating factor, eosinophil)".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.325  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.130438083  HeLa: 0.327974976  HT1080: 0.267082301  MRC5: 0.700272914  JEG3: 0.415398016  U87: 1.085691033  G402: 0.481150744  HCT116: 0.509043426  CRL1690: 0.141535029  AGS: 0.653353205  Panc1: Bad Txfn  HMCB: 0.516585685  MG63: 2.648167591  Snu-182: 1.119106205.  Number of positive cell lines: 1.  Mean: 0.846182618.  Mean(log): 0.691984554.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3567</geneId>
<geneName>IL5</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2027</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TCCATTTCAATCACTGTCTTCCCACCAGTATTTTCAATTTCTTTTAAGACAGATTAATCTAGCCACAGTCATAGTAGAACATAGCCGATCTGAAAAAAACATTCCCAATATTTATGTATTTTAGCATAAAATTCTGTTTAGTGGTCTACCTTATACTTTGTTTTGCACACATCTTTTAAGAGGAAGTTAATTTTCTGATTTTAAGAAATGCAAATGTGGGGCAATGATGTATTAACCCAAAGATTCTTCGTAATAGAAAATGTTTTTAAAGGGGGGAAACAGGGatttttattattaaaagataaaagtaaatttattttttaaGATATAAGGCATTGGAAACATTTAGTTTCACGATATGCCATTATTAGGCATTCTCTATCTGATTGTTAGAAATTATTCATTTCCTCAAAGACAGACAATAAATTGACTGGGGACGCAGTCTTGTACTATGCACTTTCTTTGCCAAAGGCAAACGCAGAACGTTTCAGAGCCATGAGGATGCTTCTGCATTTGAGTT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003462</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: RAD50 homolog (S. cerevisiae).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.588235294  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 7.483265452  HeLa: 7.406738922  HT1080: 8.852894706  MRC5: 5.584960419  JEG3: 7.737469724  U87: 7.799116431  G402: 5.8946232  HCT116: 5.904754909  CRL1690: 8.799139147  AGS: 8.883665435  Panc1: 5.912970997  HMCB: 9.711390548  MG63: 6.968820709  Snu-182: 2.657289903.  Number of positive cell lines: 14.  Mean: 239.1769499.  Mean(log): 7.114078607.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>10111</geneId>
<geneName>RAD50</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2028</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>atacacatgcgcacattccattaaccgccactgcaatggcgtcatcacatgttatgtgatcactggaaattactacacgaacgttagagagagaatgagaatgaaaaggaaaataGTTTTGACACGAACTGACCCCGCTTCCTGGGTCTCCAATCCACCCCACCACTACCCCCATTCCAGGAGTCCCAGGATCAAGCTTTGGGAAGCGCCATCCGTCACAGGTCTTGGTCTCCCCTTCCAAAAGTCAGTGCCTCTCCAGGCTGCCCATCCCCAGCAAAGATCCGGAAGTCCGCTGCCCCTGGCAACAGCACCCAGCACCTAGCCCTCTGCTTCGCCGTACCGCACCCGGAAGTCGGAGCTGCGCACGCACCGCGGGACTCTGATTTCCCGGCGTGCCCCAGGAGAGCGGCGTGGACGCGTGCGGGCCTAGAGGCCCACGTGATCCGCAGGGCGGCCGAGGCAGGAAGCTGTGAGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003463</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: interleukin 13.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.511070111  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.166054354  HeLa: 0.350294018  HT1080: 0.485285865  MRC5: 0.911259755  JEG3: 0.366355564  U87: 0.860099721  G402: 0.494975099  HCT116: 0.611660108  CRL1690: 0.679594177  AGS: 0.96512365  Panc1: 0.433779056  HMCB: 0.823543712  MG63: 0.158280418  Snu-182: 0.771882068.  Number of positive cell lines: 0.  Mean: 0.515486593.  Mean(log): 0.577013397.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3596</geneId>
<geneName>IL13</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2029</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AAATAAAACTCCCCAAATTCCCATAGCTGGTAGACTGTGGTCACAGCCACAGTGCACTAAGACTATCTGCTCAGCACTTCTGGTGACCCAAAAGGGTCTGAGGACAGGAGCTCAGAGTTGGGTCAGCTGTCCAGGTACTCAGGGTTGTCACAGGCAAAACTGCTGGAACTCAGGGCAGCATTGCAAATGCCACGCCGCTCTCAGGGCCCCTTGCCTGCCGCTGGAATTAAACCCACCCAGATCTTGGAAACTCTGCCCTGGACCCTTCTCAATAAGTCCATGAGAAATCAAACTCTTTCCTTTATGCGACACTGGATTTTCCACAAAGTAAAATCAAGATGAGTAAAGATGTGGTTTCTAGATAGTGCCTGAAAAAGCAGAGACCATGGTGTCAGGCGTCACCACTTGGGCCTATAAAAGCTGCCACAAGACGCCAAGGCCACAAGCCACCCAGCCTATGCATCCGCTCCTCAATCCTCTCCTGTTGGCACTGGGCCTCATGGCGCTTTTGTTGACCACGGTCATTGCTCTCACTTGCCTTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003464</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: interleukin 4.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.463917526  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.235271559  HeLa: 1.713377016  HT1080: 1.343827245  MRC5: 0.838348433  JEG3: 2.080716444  U87: 1.456616986  G402: 1.387862185  HCT116: 1.96147727  CRL1690: 0.998799496  AGS: 2.064184898  Panc1: 1.214438972  HMCB: 1.185330517  MG63: 1.380940395  Snu-182: 1.247902275.  Number of positive cell lines: 0.  Mean: 1.968190343.  Mean(log): 1.507792406.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3565</geneId>
<geneName>IL4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2030</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ccctgatcacaacattgcatttcagcctgggtgacagagtgagaccctgtctcagaaaaaaaaaaaaaaaaGTCATTCCTGAAACCTCAGAATAGACCTACCTTGCCAAGGGCTTCCTTATGGGTAAGGACCTTATGGACCTGCTGGGACCCAAACTAGGCCTCACCTGATACGACCTGTCCTTCTCAAAACACCTAAACTTGGGAGAACATTGTCCCCCAGTGCTGGGGTAGGAGAGTCTGCCTGTTATTCTGCCTCTATGCAGAGAAGGAGCCCCAGATCAGCTTTTCCATGACAGGACAGTTTCCAAGATGCCACCTGTACTTGGAAGAAGCCAGGTTAAAATACTTTTCAAGTAAAACTTTCTTGATATTACTCTATCTTTCCCCAGGAGGACTGCATTACAACAAATTCGGACACCTGTGGCCTCTCCCTTCTATGCAAAGCAAAAAGCCAGCAGCAGCCCCAAGCTGATAAGATTAATC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003465</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "CDNA clone IMAGE:4831161, partial cds".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.365269461  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.103228134  HeLa: 0.695611598  HT1080: 0.557254058  MRC5: 1.059438567  JEG3: 0.397110144  U87: 1.108497416  G402: 0.484434659  HCT116: 0.503103703  CRL1690: 0.742452905  AGS: 0.597512185  Panc1: 0.446298573  HMCB: 0.621100591  MG63: 0.251158665  Snu-182: 1.140613773.  Number of positive cell lines: 0.  Mean: 0.572880489.  Mean(log): 0.621986784.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC033341</geneId>
<geneName>BC033341</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2031</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGCTTTGCAAATGAAACAGCTTAAGACAGAGAAATTGAGATAATAATTAATAAATGTGTTTGGAAGGCTCCTCCAGCTCGCTTTAAGTTCAGGCTGTGGCTTCAGAACTGTGTTAACTCCTTCTGTAAAGGCACAGGCTAACGGTGGTCTTCAGTGATTTTTACTCTACCTTGTTTTAAAAATGGATTCAAAGTGATTTATTGGAAAAGATTAAGACAGAAAATAACATTATTAGGACCAAAGCAGAAAGGGAGTAGGAGGAAATGATGATCCAGAGAAAAATAAGACTATAAGCAGGTCATCAGATATTATAGTCCTATCAGCAAAAGCACAGTGGAAAACGCATTATTTTACTTCACTCTTTTTATATATGCGGGGAGAAAATAGTCTGATATAATAATCTGGTACTTAGCTTTAAAAGAAATTTCTCGAGAATCTTCACAAGATGATAGGATGGACAATGTCTTCAGCAGCATCCCGACAACACAGGCAGTAACAGAC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003466</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: kinesin family member 3A.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.554865424  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 7.978088965  HeLa: 7.115487125  HT1080: 7.102486415  MRC5: 4.981572835  JEG3: 7.046804431  U87: 7.431472482  G402: 6.259547353  HCT116: 5.752684519  CRL1690: 5.985701353  AGS: 7.183442786  Panc1: 5.402865304  HMCB: 8.243756057  MG63: 4.732978907  Snu-182: 2.952957923.  Number of positive cell lines: 14.  Mean: 112.1209086.  Mean(log): 6.297846175.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>11127</geneId>
<geneName>KIF3A</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2032</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>gggctctggagatagatgtgagaatactaacaatctccttaagagagctcactttctaatggtaagacaGGTCATGAGGAAGTTAGCAATCAAGCGAGGTCAGGTAGGTAAGGTCTTCAATTCTTCGGATGAGACAAAATGTACAATTGCTATTACTGATTTTAATATTCCGGGTATTGCAAGGGCCAGAAGACGGGCCTAAGAGCAGCTCCTCCTCCCAACCCCGGGCTGCCAGGTTACCTCCGCCTCAGTGCGTGCCACATTTCTAGCGCAGCAGAATGGCAGCATTGCGCACGCGCGGCCTCAGTCTGGCGTCCTAGGAGATGGACTCGGAAAGCCTCCGCGCAGGCGTAATTCAAGGGCCGAGAGAGCCTGAGACTGGGCTTGGGGCGGGGCGAGCTCGGAATGCGGCTGCGCACTGGGCGCTCTCGCCCGAGAAGCCGCAGTCTCGAGAGCGTCAACGAGGTGTTTCGGTAGTCTCTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003467</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: septin 8.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.582969432  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.842872954  HeLa: 1.584571822  HT1080: 1.869533816  MRC5: 1.022442744  JEG3: 1.198371044  U87: 2.059651957  G402: 2.695157619  HCT116: 2.356452764  CRL1690: 1.365173737  AGS: 1.716987203  Panc1: 3.315027909  HMCB: 1.82057795  MG63: 2.596325797  Snu-182: 1.306385345.  Number of positive cell lines: 5.  Mean: 3.029145956.  Mean(log): 1.839252333.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>540614</geneId>
<geneName>LOC540614</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2033</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTTGGGGATCAGATCAATAAGGATGAGAGGCAAGAGGCGGGAAGGGCGGCCCCACCCAGCCTCCTCCCACCCCACCTACATTGGCCCCTATAACAGTAGCCCAGCCCTCACACTGCAGGGGGCCAGGGAGGGCCTCTTGGGGAATATCTGAGGCTCTGTGGTCACCAACAGACCAGTTACTCCTTTAGGTGTCTGGAGAAGGGGTCAGCTGCCTGTATCCAGTCAGGGATCTCAGGCAGAAGCTGTTCCCAGAAAGAAAAGGCCAGGGGGCAGCCTGGCTTGGCCCCGAGCCCTGAGCCCCCCAAGCCCCAAGCCCCTGATCTCAGCTGGCAGCCTCCTGGGTGATGGAGCTGTCTGTAGTTACAGGCCCATAGTTGACTACATCGATGCGCAGTTTGAAAATTATCTGCAGGAGGAGCTGAAGATCCGCCGCTCGCTCTTCGACTACCATGACACAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003468</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: septin 8.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.567901235  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.830303199  HeLa: 1.167367501  HT1080: 1.049412087  MRC5: 1.295561336  JEG3: 1.262074393  U87: 1.762915167  G402: 1.425479481  HCT116: 1.347917881  CRL1690: 0.950182854  AGS: 1.143123016  Panc1: 1.524870854  HMCB: 1.315959757  MG63: 1.260917199  Snu-182: 0.981570092.  Number of positive cell lines: 0.  Mean: 1.389377782.  Mean(log): 1.236975344.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>540614</geneId>
<geneName>LOC540614</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2034</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTCCCAGAAAGAGCAGAGAGAAAGGCAGAGGGAAGAGAAAGAAACGGGGTTTCAGAGGATTTGGGAGCTGCTTTTGTATAGATTGTCAGTGAGAAGGATACAGAACCTCCTGAGGCCTCCGACCCTGGCGTAAGTGTTAATTTTCTGAACGTTTTGAGCAGTGACATTAGCGGAGAGAACGTGCACGCACTGGGAGTGGTCATCCTCTTTGCACAATGGTGGAACCATTAAGACGTTGTCCCAAGCCCTTGGGACAGGCAGGGTGATGGACACTTGCAATCTGACGCCTTGACCGTCGAGCTCCGCTTTTCTATTGCAGGAATCCCAGCCTAAACTGCGCATCCTGCTCGTTGGTTGCACAAGGAGCCGAAGGCTGGTCCCTTGCCCGGGAAGGCCGCCTGGCCGGACGCGCGGGTCCCGCCGGGGTTCCCGCCTTAGCTCCGGCCGGAGCATCAGGTGGGGCCCAAGACACCCGCAGACTAGGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003469</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: apical protein 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.540892193  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.22325663  HeLa: 0.652114321  HT1080: 1.005200373  MRC5: 0.887428301  JEG3: 0.356191783  U87: 1.07637907  G402: 0.899083612  HCT116: 1.303438086  CRL1690: 0.914908207  AGS: 0.821843043  Panc1: 0.767378185  HMCB: 0.77998444  MG63: 0.611103441  Snu-182: 0.95155275.  Number of positive cell lines: 0.  Mean: 0.775109657.  Mean(log): 0.803561589.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>NM_133456</geneId>
<geneName>NM_133456</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2035</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ttccctctcagaacctcattgtccttgtctgtaaaatgcagacagcagttgcaacgatcaaaataaatatttatataaagcacctggaacataacaggcacagagGGAGGGAGGAAGGCTGTGAAGCTGCCTCTGCCCCTTGCCCTGGGTCTTCCCCCACCCCTCCTTTCTTAGCTCCCCTGAGGTCACAAGAGTGTTCTTGACCATTGTTTATCAGGGAAAGATCACATGGAGAAGCCAACAGAACGGCCAGGAAGCAGCCTGGGTGGAACAGGGTTGGGGAGGAAAGGAACATGGGTACATTCTCAGCGTTCCAGGAGGTCTCAGGGTAAAGGCTGCTTGTGTGGGCAAGGGGAGCCTGGCAGGGAATGAGCTGGTCCCAATTCCTTCCCCTGAGCTGGGCCCTCAACCTTCAGAGGTGCTCCCTGGGACTGGTCCTACTTCCTCTGCCACCTCTGATCCCAAGGTGACTCTGCCAAAATCTGGGGGATGCCAGCGCTTGTGACGGTGTGACCAGGGAGGGGAAGTGTAAGTGTCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003470</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: growth differentiation factor 9.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.406882591  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.193607646  HeLa: 0.47439339  HT1080: 0.48027394  MRC5: 1.147912978  JEG3: 0.470109289  U87: 1.12396395  G402: 0.735919587  HCT116: 0.82417701  CRL1690: 0.390809364  AGS: 1.486142417  Panc1: 0.552621851  HMCB: 0.671402023  MG63: 0.459965352  Snu-182: 1.161376508.  Number of positive cell lines: 0.  Mean: 0.709188846.  Mean(log): 0.726619665.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>2661</geneId>
<geneName>GDF9</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2036</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GCCTTAGAAGTTTCAGCAAGCACCTAGCGAACATCTTAATCCAAATTTCTCAAAAAATGAGAGATTTTATTTAAGATCATTCCTCAATTTATCTTAGACTTTCAGCTACATAGTTAGTCCGGTAGTGTAACAGTAACGGGTTTTACGTAAATGCCAGGGGAAAAGAGAGGAAAGCTAAATAACCAAGTAAATCTGTATCTAATTAACAAATTGGCTAAATAAGGTGTTATCAGCTGCTTGATATAGAGCTGATAAAATCTTCAGCTAGGCATACTTGAGGCCTGATTACAGAAGTGACCGTAGTCCACCCACACACCTGAAATTTATTTAAGAGACCAAGCTAGGCTCTTCCTGGCCTTTAGGAAGAGGACTGGCATGGAGAAATATGTTCCTCACTAGTTCTCCCAAGCCATGGCACGTCCCAACAAATTCCTCCTTTGGTTTTGCTGCTTTGCCTGGCTGTGTTTTCCTATTAGCCTTGGTTCTCAGGCTTC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003471</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: low molecular mass ubiquinone-binding protein (9.5kD).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.621900826  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 9.567755078  HeLa: 8.835929937  HT1080: 9.717385188  MRC5: 7.270095055  JEG3: 10.47664533  U87: 10.04330927  G402: 6.806393463  HCT116: 7.522809329  CRL1690: 9.786151579  AGS: 10.80922439  Panc1: 6.194615991  HMCB: 10.16764906  MG63: 9.039309518  Snu-182: 5.976741944.  Number of positive cell lines: 14.  Mean: 675.9837823.  Mean(log): 8.729572509.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC064949</geneId>
<geneName>BC064949</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2037</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CTGTCTACAGCTGGGAAGACTCGCAGGCCCCAAGCTCCTGGCCAGCGCTGCCCCGGAGGTCGGCAGGCCCCTTCCTCGTCACCTTTTTGTTCCCTCCCCCGCCTCCCGCATTCGGCCGCTTCCTGACTGGGATTCCACAGAAAAGCCGAGGGCTGAGGAGAAGTGTGAGCGCCTCCGCCTGTCCACTGTCCCCCAAAGTCAGTTCAATCCCCGACGTCCTCCGCTAGGCTCCACCCCACCGGCCCGGGCAGGGCCTCCAAGGCACCTCCCACCTACGGGTCACCCAGTCAGCCCACTTCTTTCTGGGACAAAGGCGTCATCCCTTAGAGACAGTAGGAAAATGGTATCTCCCGGAAGTTACCTCACGACCTCCAAGAGCGGCTTCCAACCTTGCCGGAAATGACGAACGAGTCAACCGGATCGGTGACTGTGGAGGGCGAGCTGAGCCCTGTGCGTGAGTGGGGTCTGGTTGTGCAGTGTTCGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003472</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: liver-expressed antimicrobial peptide 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.488469602  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.291649932  HeLa: 1.054477963  HT1080: 0.751191021  MRC5: 1.021797646  JEG3: 0.488407357  U87: 1.465086727  G402: 0.817065291  HCT116: 1.057722576  CRL1690: 0.790928854  AGS: 0.614256534  Panc1: 0.818148708  HMCB: 1.042319713  MG63: 0.712618638  Snu-182: 0.953410193.  Number of positive cell lines: 0.  Mean: 0.834332034.  Mean(log): 0.848505797.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>NM_052971</geneId>
<geneName>NM_052971</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2038</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AGGCAGAAATGGAGGATTAGGAGAATTACTCATCTTTTGGATGAACAGTTTCCAAATCCCATTTGGCACATCACTCTAGACTGGTAAAGGGGAGGCTGACACTGAGGCCACAGACCCAACTGGCTCTAGGACATCACGTTGTTCAGTCCTTTGCTTATCTAATCATTTGTGTTCTTACCCAGTGCTCACTAGGTCACCCACATAGCCACTTCCCCTCCCAGCAAAAGTTCCCAGTTTAGGCACCTGTCTGGGATCATCCAGTATCCAAGCTTAGGGGTGAAGGGAGGGAGCAGAGAACTAGTCTCAACTGGTTCGTTGGTATATAGGTCTCTTCTCAATGTTCCTAAAGTGCATGCAGTGGCATCCCCCTCAAGGCCTGGCTCCATGATTCTGAGAGGACTAGAATCAGGACAGTCAGATCTGTGGTCACATCCTGCCCAATTCCAGCTCTGAGGTCCATCAAACCATCTGCTTCTC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003473</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: ALL1 fused gene from 5q31.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.339181287  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.170235255  HeLa: 0.705697404  HT1080: 0.59415296  MRC5: 0.932381858  JEG3: 1.111591709  U87: 0.962418396  G402: 0.807628935  HCT116: 1.021424403  CRL1690: 1.194764637  AGS: 1.220457061  Panc1: 1.116508147  HMCB: 0.882254385  MG63: 0.948713256  Snu-182: 0.796109261.  Number of positive cell lines: 0.  Mean: 0.963314686.  Mean(log): 0.961738405.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>27125</geneId>
<geneName>AFF4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2039</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTAATGTTCAAGGGTGCAATGTGTATTCCTTTAGATTGTTAAAGCTTAATTACTATGATTTGTAGTAAATTAACTTTTAAAATGTATTTGAGCCCTTCTGTAGTGTCGTAGGGCTCTTACAGGGTGGGAAAGATTTTAATTTTCCAGTTGCTAATTGAACAGTATGGCCTCATTATATATTTTGATTTATAGGAGTTTGTGTCTGGGTCCCAGGAACATCTACTGGGGATGACTGTTAGGCAGCTTGTGATGATGTTTTTTAAAAAACCTAAGTAACTTGGGGAGACAGAGCATTTCAAACCCATATAGACACCTATCATACCTGTATATCCCCTAATACATGGAACATAAATTTCATTTCAGCTTTATGCATTAATGTATTGAAGAGGCAGGCTTTTTTTCCAGTAATAATACTGTACATCTAAGGTTGCTATTCAGTAAAACTAATAGAAGAGATAATTATTGAATACCTTGGAATATGTAGTGAGAAGAGGCCAAATTTTTCATGTTTGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003474</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: ALL1 fused gene from 5q31.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.307692308  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.40467723  HeLa: 0.401824624  HT1080: 0.56848237  MRC5: 1.168210172  JEG3: 0.622259356  U87: 0.990729429  G402: 0.405972953  HCT116: 0.682440698  CRL1690: 0.207198092  AGS: 0.638609973  Panc1: 0.357111156  HMCB: 0.846423107  MG63: 0.500114407  Snu-182: 1.167889421.  Number of positive cell lines: 0.  Mean: 0.591635013.  Mean(log): 0.640138785.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK129636</geneId>
<geneName>AK129636</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2040</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>caagtttatcttgccaaatcccaggtcatttagatttggcattgtgtttttttctaaagattttatagctctagcttttacatttataggtctttgatccttcttgagttttttgttttgttttgttttgtttttaatatgatgtgatataaaggcccagctttattttgcccatggatattcagtttgtccagcaccgttgttaaaaagactattctttcccatataatggtcttggcatcctcttggaaaatcagttgaGTGTAGAAATAGGTTTTTAATGTTTTTTAACCGCAAAACTATATTTTAGCTTTCTAACTATTTGGATTGTTCTTTCACAGACAATTCTGTAACTAAAGGAAGATTATGCTTATTTTTAAGTAAGCTTTTAGGAATATTTGTATAATTTTAGTGCTACATCTTGTATCCAGATTTAATTTTGAGAAATGCATAGTTTGCACATATGGAACAGCTGTTCTGGTCATGAAAATTGA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003475</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "interleukin 3 (colony-stimulating factor, multiple)".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.55179704  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.423515044  HeLa: 1.465054399  HT1080: 2.46789168  MRC5: 1.338403549  JEG3: 1.135855936  U87: 3.32432624  G402: 1.401731754  HCT116: 2.408386081  CRL1690: 1.778915016  AGS: 2.574528184  Panc1: 1.506131853  HMCB: 1.962447358  MG63: 0.748487854  Snu-182: 0.989294593.  Number of positive cell lines: 4.  Mean: 2.722820634.  Mean(log): 1.680354967.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>3562</geneId>
<geneName>IL3</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2041</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CGGCTACCAGACAAACTCTCATCTGTTCCAGTGGCCTCCTGGCCACCCACCAGGACCAAGCAGGGCGGGCAGCAGAGGGCCAGGGTAGTCCAGGTGATGGCAGATGAGATCCCACTGGGCAGGAGGCCTCAGTGAGCTGAGTCAGGCTTCCCCTTCCTGCCACAGGGGTCCTCTCACCTGCTGCCATGCTTCCCATCTCTCATCCTCCTTGACAAGATGAAGTGATACCGTTTAAGTAATCTTTTTTCTTGTTTCACTGATCTTGAGTACTAGAAAGTCATGGATGAATAATTACGTCTGTGGTTTTCTATGGAGGTTCCATGTCAGATAAAGATCCTTCCGACGCCTGCCCCACACCACCACCTCCCCCCGCCTTGCCCGGGGTTGTGGGCACCTTGCTGCTGCACATATAAGGCGGGAGGCTGTTGCCAACTCTTCAGAGCCCCACGAAGGACCAGAACAAGACAGAGTGC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003476</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: colony stimulating factor 2 (granulocyte-macrophage).  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.570576541  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.24197825  HeLa: 0.947245852  HT1080: 3.810574992  MRC5: 1.576447004  JEG3: 0.487496139  U87: 3.421514652  G402: 1.266512191  HCT116: 2.756370393  CRL1690: 1.915390427  AGS: 3.716137108  Panc1: 1.68978451  HMCB: 1.474859549  MG63: 1.442497696  Snu-182: 0.933243224.  Number of positive cell lines: 5.  Mean: 4.009568068.  Mean(log): 1.905717999.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>1437</geneId>
<geneName>CSF2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2042</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CCCTCACACTCAAGTCTCTCACAGTGGCCAGAGAAGAGGAAGGCTGGAGTCAGAATGAGGCACCAGGGCGGGCATAGCCTGCCCAAAGGCCCCTGGGATTACAGGCAGGATGGGGAGCCCTATCTAAGTGTCTCCCACGCCCCACCCCAGCCATTCCAGGCCAGGAAGTCCAAACTGTGCCCCTCAGAGGGAGGGGGCAGCCTCAGGCCCATTCAGACTGCCCAGGGAGGGCTGGAGAGCCCTCAGGAAGGCGGGTGGGTGGGCTGTCGGTTCTTGGAAAGGTTCATTAATGAAAACCCCCAAGCCTGACCACCTAGGGAAAAGGCTCACCGTTCCCATGTGTGGCTGATAAGGGCCAGGAGATTCCACAGTTCAGGTAGTTCCCCCGCCTCCCTGGCATTTTGTGGTCACCATTAATCATTTCCTCTGTGTATTTAAGAGCTCTTTTGCCAGTGAGCCCAGTACACAGAGAGAAAGGCTAAAGTTCTCTGGAGGATGTGGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003477</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide II".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.558333333  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.576606195  HeLa: 0.795983058  HT1080: 1.292209055  MRC5: 1.307593006  JEG3: 0.689413451  U87: 1.384909711  G402: 1.020224155  HCT116: 1.284731907  CRL1690: 1.173943511  AGS: 1.165198414  Panc1: 1.592741549  HMCB: 1.372562274  MG63: 1.689324044  Snu-182: 1.105590566.  Number of positive cell lines: 0.  Mean: 1.308718148.  Mean(log): 1.175073635.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>8974</geneId>
<geneName>P4HA2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2043</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AAGTCTTTTCTCCCCCAGACATCCTTGTGGAACCAGCGTTGTTTTTCCTTGGCAGCTGCGGAGACCCGTGATAATTCGTTAACTAATTCAACAAACGGGACCCTTCTGTGTGCCAGAAACCGCAAGCAGTTGCTAACCCAGTGGGACAGGCGGATTGGAAGAGCGGGAAGGTCCTGGCCCAGAGCAGTGTGGTGAGCGCTGTGCTGGAAGGGAATGCGGGCAGTGGGTACTTGGTAGAGCACTGACTGCCTCCGGCCAGAGGACTTCCCGGAGGAGGTGACCCATGAGCTGGAGTGGTCAGAGGAAGGCTGGCAAAAGGGCATCGTGGACAGAGGAACAGCCTATGTGAGTGGGAGCAGAGACCTTGGCCAATGCCATTCCTTATGGCCTTGTAGTGGAAGCAAGGTGATGGGGAAGGAACACTGTAGGGGATAGCTGTCCACGGACGCTGTCTACAAGACCCTGGAGTGAGATAACGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003478</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide II".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.743636364  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 6.149162706  HeLa: 4.802430284  HT1080: 5.438170142  MRC5: 4.316000741  JEG3: 4.7788327  U87: 4.605608252  G402: 4.968886356  HCT116: 4.300849832  CRL1690: 3.662433751  AGS: 4.450705959  Panc1: 4.991518657  HMCB: 4.82102634  MG63: 4.626144745  Snu-182: 1.529002987.  Number of positive cell lines: 13.  Mean: 26.65459393.  Mean(log): 4.531483818.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>8974</geneId>
<geneName>P4HA2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2044</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TAACAGCCTCCTTGTGGTGGTGCTGGGAAGAAGGGGCCCGTGTACCCGGCAGGGCCCCCCAGGCAATGGGCATGAGCGCAGGCAGGGAAATCCGTCAGCCTCCAGGGACGCTCTCCCTACAGCCCCGGCGAGGGGATCGGGTCGTGGCGACCTCTCCAGACGCCCAGGGGCTGGGCAGGAGGGCGGGCCAAGGCCCGCAGGTGGGGGCGCCAAAGCCAGGCGGGCGCGGAGTACGTGCGGTGGGCTGCGGGCGGCATGAAGGGCGCGGGCGGCCAGCTCCGGCTCCGGCTCCGGCTCCGGCTCCCGCGAGGCCGGGTAGCCTGGGCGTTCCCAGGGGTCGCAGAGGACGGCGAACCCCGGCGGAGCCACCGGAGCTGGGGACCAGGACGCAGGCAGGCGTGTGGAGCGTGAGGTGGGGACGTGGCGGCGGCTCAAGTGGGCGGAGCCCCGGCAGCGGCCCGAGGCGGAGTCGCCAAGGGAGGAGGCGCCGAGCTGACCGGGCGACGCCGCGGGAGGTTCTGGAAACGCCGGGAGCTGCGAGTGTCCAGGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003479</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: PDZ and LIM domain 4.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.733059548  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.937871764  HeLa: 1.805311616  HT1080: 2.792074732  MRC5: 1.653564005  JEG3: 0.910379751  U87: 1.609698132  G402: 1.562533021  HCT116: 1.578347643  CRL1690: 1.236307026  AGS: 2.021877758  Panc1: 1.416216824  HMCB: 2.574886125  MG63: 2.602532933  Snu-182: 1.060762249.  Number of positive cell lines: 5.  Mean: 2.95038007.  Mean(log): 1.840168827.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>8572</geneId>
<geneName>PDLIM4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2045</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TCATAGGGTTCTTGGTTCAGAGGGCTCCTCACACGGCAGGATGGGCCGCAGGTGTGCCAGTCGGGCCCATGAGGAGGTATCTGAGCTGGGGCAGCCCCATCCCCCAAGTGGGCCCTCCATCCCTCCTCGGGCTGGAGCACCGCCCCTAAAAGCGACTTCAAAGGGCCGGTGTCGACAGCTGGGTTTGGGTCCGCGGCCTGCAGATCCAAGGCCCGAGCAGGATCCAGGCCGTCGGGGCCGTCCGAACGCGGGGATCTCTGAGAGCTGAGTGGGGGTGCCGGGTTGCCGGCAGCCGGGGCTGAGGGCGGGTCCTCAGAGCCCCCCGAAGTGGGAGGGTCGGGCTGGCCGCGGGGCCAATCCAGGCGCACAgggagcgggggcgggggctgggccgagtggggacaggggcgggcgggccgggggcgggcgcggCGTCCAggcggcggcggcggctgcggcggcggcggcTCCTCCTCAGAGTCCGGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003480</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: hypothetical protein MGC13125.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.656387665  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 7.003557916  HeLa: 5.642434964  HT1080: 6.81542125  MRC5: 3.881425776  JEG3: 5.668638945  U87: 6.826540353  G402: 4.083496689  HCT116: 4.660125954  CRL1690: 6.489046682  AGS: 6.512880796  Panc1: 4.51629849  HMCB: 9.056370535  MG63: 5.142896329  Snu-182: 1.95001935.  Number of positive cell lines: 14.  Mean: 90.99020568.  Mean(log): 5.589225288.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>NM_032725</geneId>
<geneName>NM_032725</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2046</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>cagtattcaaactcggctacgctgcagcccgtggccctccactTTCTTGCTCGTGCTCTGGAGTTTAGGCGGCCGATGGGGGCGGGGTCCTTTGGGTCAGGTTGTGGCCTCATAGAACAGCGCTTGCTGCGGTtggatggatgggtgggtgggtgggtgagtgAATGAAGAGAAGAAACCTGGTGGCGTCGTCCCAGGGCTGTGGAGCGCCCCGAAGGTGCGCACGTCCCTGGCTAGCCTGCGAGCGCGTCCCGGTGGCCGCACCTGCCAGCCGCGCGATTCTTAGCACTCTCCGCCACTTCCGGCCGTGGCCCCGCCCTGTCGGGTGGCTGGCGTCCGTTACGCGTTGAGGCATTTTGTCCCCAGCGCCGACCCGTCTCTCTGCCCCCGCCGCTGCCATGGCGGCAGCTCCGCCGCTTTCCAAGGCCGAGTATCTGAAGCGTTACTTGTCCGG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003481</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:5288763, mRNA".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.427368421  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.718115734  HeLa: 1.298819232  HT1080: 0.911561556  MRC5: 0.998989122  JEG3: 1.894541651  U87: 0.904511984  G402: 1.267970482  HCT116: 1.264472322  CRL1690: 0.913869493  AGS: 1.295732911  Panc1: 1.235012939  HMCB: 0.998645492  MG63: 1.317510989  Snu-182: 1.090938828.  Number of positive cell lines: 0.  Mean: 1.381724044.  Mean(log): 1.222192338.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC042385</geneId>
<geneName>BC042385</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2047</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGGCGAACTTTAAAACCATCAGTGATTTGAGTTAATTCTACCTGTTTTACCTTATTTTTCACCAGTGTGTGTTTCCTCACTGCCTCATTATATTGCCACATTTAATCTTTCATTAAAACAAACAAACAAACACAACTCTTggctgggtgtggtggctcacacctgtaatcccggtactttggaaggctgaggtgggaggattccttgagttctagaccagcctggtcaacatagggagattctctctctcctgaaaaaaaaaaaaaaaaaaaaaaattaaccaagcatggtggcacacatctgtagtcccagctactcaataggcaaagtgagaggattgcttgagcctgggaggttgaggctgcagtgaacatgatcaaaccactgcattccagcctggaggacagagcgagaccctgtcttacaaaacaaaaCAACAACTCTTGGAATttctcttttcccctcccttcttctt</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003482</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:5730164, mRNA".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.488372093  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: Bad Txfn  HeLa: 2.659656589  HT1080: Bad Txfn  MRC5: Bad Txfn  JEG3: Bad Txfn  U87: Bad Txfn  G402: Bad Txfn  HCT116: Bad Txfn  CRL1690: Bad Txfn  AGS: Bad Txfn  Panc1: Bad Txfn  HMCB: Bad Txfn  MG63: Bad Txfn  Snu-182: 1.13018838.  Number of positive cell lines: 1.  Mean: 3.253849708.  Mean(log): 1.894922485.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC035670</geneId>
<geneName>BC035670</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2048</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ttacaggtgacaaaacagcctcagagaggttaCTTCCAGAAGGAAGCAGAGCTTTTTttttttttttttttttttttttttttttttgagacggagtctcactctgttgcccagactggagtgcagtggcgtgatcttggctcaccacaacctctgcctcccaggttcaagcgattctcttgcctcagccttctgagtagctgggactacaggtgcacgccaccatgcctggctaattttttttttttttttttttttggagacagtcttgctctgtcacccaggatggagtgcagtggtgcgatcttggctcactgcagccttgcctcctgggttcaagcaattctcctgcctcagcctcctgagtagctgggattacagacgcccaccactgcacccagctaatttttgtatttttagtagagatggggtttcaccatgttggtcaggctggtctcaaacccctgacctcgtgatccacctgccttggcctcccaaagtgcagggattacaggc</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003483</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: zinc finger protein 259.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.597916667  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 9.402312863  HeLa: 8.272028735  HT1080: 7.974991839  MRC5: 6.552261215  JEG3: 8.734222141  U87: 8.829613033  G402: 5.343445087  HCT116: 6.514770632  CRL1690: 8.30972651  AGS: 9.271411015  Panc1: 5.182201445  HMCB: 8.027831946  MG63: 8.396107902  Snu-182: 4.422423533.  Number of positive cell lines: 14.  Mean: 280.07212.  Mean(log): 7.516667707.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>8882</geneId>
<geneName>ZNF259</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2049</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GAACAGAAAGGGACAGAGGGATTCAGGGATTGTGAGAGAGGGGAAGAGGCTGAGCCACCCGGAGGGGCGACCTAGCACGCAAGCAGTATGTGGCCCAACACTGGAACCAAGCAGCCCGGCTCCGGGCGCACCTTCTCAGGGATTCCTCAGGGACAAGTCCAGCCCCTTGTCGTCAAGGCTCTTGTAGACCGACGTAGGGACCAATAGAACCCCGTGCGGTGGAGCTATTGTGAAGGAGCAAAAAAGTGCCCTGGTTCTAAGAGGACGTCTTAGGGGAAGTGACGGCTGAGTTGAGGTGGATCCGGCTGGCGATGTAAGGTTCGAGCCATATAAACCCGGGAACCGGGAGCCCTTGACGACATTGTTCCCCGAGTGCCCGGAGTCTGCGGCTTTTTTTGGGGTGGTGGCAGCTGGCGGAAGTGACGGGAGAGGGGTGGGGCCGCGAGAGCGGCGGAAGTAGGAAGCCGAGGTCTGAATTGC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003484</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: apolipoprotein A-V.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.582120582  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.915819604  HeLa: 0.433704691  HT1080: 0.379321447  MRC5: 0.881052486  JEG3: 1.167306956  U87: 0.583874974  G402: 0.715210778  HCT116: 0.88279258  CRL1690: 0.916482704  AGS: 0.708984486  Panc1: 0.34234911  HMCB: 0.677154037  MG63: 0.773576907  Snu-182: 1.280730613.  Number of positive cell lines: 0.  Mean: 0.724166177.  Mean(log): 0.761311527.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>116519</geneId>
<geneName>APOA5</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2050</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TCTTGGAACATTTTGGCAGAGTTGCCTCTTCGCCCTCATTATGGCTCAGTTTTTCCACCATGAAATGGGAGGGAGGGAGACAGGTGGGCAGGGGAGAGGTGGTAGAAGTGGCCTAGAGAACTGTTCCTGGGGTCTGGGACCTTTGCGAAGGGGTTAGAGCACCACGCTCCCTGCTATGTGACTGAGGTAGCAAGAGCACGCCCTCTTCCCATGTCTGAGGAAGACACCCTAGCCTCCTTGACTCACCTAGGTCAGTCCTCTTGAGCCCCAACAGCTCTGTGCTCCCCAGCCCAAGGAAGGGGTAACAGGATTTCGGGCAGTTGCCCCTGCAGAGGCCCCCTGGGCAAGTCCCCTGCGCCATGTCCCTTCGTCTCCTTCTTCCCCTAACCAGGCCTCCCTCCACCTGTCTTCTCAGAGCAGGTAATGGCAAGCATGGCTGCCGTGCTCACCTGGGCTCTGGCTCTTCTTTCAGGTGGGTCTC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003485</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: apolipoprotein A-IV.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.600840336  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.262998308  HeLa: 2.062093656  HT1080: 3.596407869  MRC5: 2.597641006  JEG3: 2.525981233  U87: 4.938386196  G402: 4.37804075  HCT116: 4.707572259  CRL1690: 3.83718316  AGS: 4.389766969  Panc1: 2.834929273  HMCB: 2.197993883  MG63: 2.793315707  Snu-182: 1.886686076.  Number of positive cell lines: 11.  Mean: 11.00550839.  Mean(log): 3.21492831.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>337</geneId>
<geneName>APOA4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2051</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CACTGGGGTAGACAGAGGAGATGTGGACTTTGCCCCCCATGAGCCCGGCACAAACCCAGAGCCGCCAGCAGGGCCTCGAGGCATCAGTCCCGGGCTCATGGGCTCCCTGAGGTGTTTCTCCTACTGTTTTCCGTTCCCCTCCTCCCTTCCATGCTGAGGTTGGTGGGGTGGGGGTGGGGGTGCCCACGCACGGAACAGCCACCACTTCTAACTATCGCCTGAGCCCTGATCTGCTGTCAGCTTCCACGTAGTCTCAGGGTCACAAAAGTCCAAGAGGCCTCTTGGGAATGTGTCACCTTCCAGCGTGGAGTCACACTGAGGAAGGAGGAGGGGAGGGCAGCCAGGGGGGTGGCGATAGGGAGAGAGTTTAAATGTCTGGCTGGCTCTGAGCTTCAGTCAGTTCCCACTGCAGCGCAGGTGAGCTCTCCTGAGGACCTCTCTGTCAGCTCCCCTGATTGTAGGGAGGATCCAGTGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003486</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: apolipoprotein C-III.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.613537118  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.638472718  HeLa: 1.728416633  HT1080: 2.033489258  MRC5: 1.539692959  JEG3: 2.385366696  U87: 2.35167165  G402: 2.334979113  HCT116: 2.301912993  CRL1690: 1.057184419  AGS: 2.119572055  Panc1: 1.591109098  HMCB: 1.704625272  MG63: 2.631773812  Snu-182: 1.087788806.  Number of positive cell lines: 5.  Mean: 3.133515549.  Mean(log): 1.964718249.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>345</geneId>
<geneName>APOC3</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2052</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGTTCTCAAGTCTGAAGAAGCCCCTCACCCCTCTACTCCAGGCTGTGTTCAGGGCTTGGGGCTGGTGGAGGGAGGGGCCTGAAATTCCAGTGTGAAAGGCTGAGATGGGCCCGAGGCCCCTGGCCTATGTCCAAGCCATTTCCCCTCTCACCAGCCTCTCCCTGGGGAGCCAGTCAGCTAGGAAGGAATGAGGGCTCCCCAGGCCCACCCCCAGTTCCTGAGCTCATCTGGGCTGCAGGGCTGGCGGGACAGCAGCGTGGACTCAGTCTCCTAGGGATTTCCCAACTCTCCCGCCCGCTTGCTGCATCTGGACACCCTGCCTCAGGCCCTCATCTCCACTGGTCAGCAGGTGACCTTTGCCCAGCGCCCTGGGTCCTCAGTGCCTGCTGCCCTGGAGATGATATAAAACAGGTCAGAACCCTCCTGCCTGTCTGCTCAGTTCATCCCTAGAGGCAGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003487</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: apolipoprotein A-I.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.626  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 7.734055597  HeLa: 2.826770438  HT1080: 3.492404187  MRC5: 2.004008787  JEG3: 1.951000297  U87: 3.125281844  G402: 3.289976238  HCT116: 2.643197494  CRL1690: 1.759152107  AGS: 2.81830397  Panc1: 3.200588438  HMCB: 3.505374474  MG63: 2.589905753  Snu-182: 1.570539742.  Number of positive cell lines: 12.  Mean: 20.70445509.  Mean(log): 3.036468526.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>335</geneId>
<geneName>APOA1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2053</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AGGGGAGTGAAGTAGTCTCCCTGGAATGCTGGTGGTGGGGGAGGCAGTCTCCTTGGTGGAGGAGTCCCAGCGTCCCTCCCCTCCCCTCCTCTGCCAACACAATGGACAATGGCAACTGCCCACACACTCCCATGGAGGGGAAGGGGATGAGTGCAGGGAACCCCGACCCCACCCGGGAGACCTGCAAGCCTGCAGACACTCCCCTCCCGCCCCCACTGAACCCTTGACCCCTGCCCTGCAGCCCCCGCAGCTTGCTGTTTGCCCACTCTATTTGCCCAGCCCCAGGGACAGAGCTGATCCTTGAACTCTTAAGTTCCACATTGCCAGGACCAGTGAGCAGCAACAGGGCCGGGGCTGGGCTTATCAGCCTCCCAGCCCAGACCCTGGCTGCAGACATAAATAGGCCCTGCAAGAGCTGGCTGCTTAGAGACTGCGAGAAGGAGGTGCGTCCTGCTGCCTGCCCCGGTCACTCTGGCTCCCCAGCTCAAGGTTCAGGCCTT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003488</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0999 protein.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.44375  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 3.045617686  HeLa: 2.150530385  HT1080: 2.106632075  MRC5: 1.204832364  JEG3: 2.524683575  U87: 1.940151173  G402: 2.197791875  HCT116: 2.871575978  CRL1690: 1.442531987  AGS: 2.332943141  Panc1: 1.849774488  HMCB: 1.95292883  MG63: 2.622243897  Snu-182: 1.173162528.  Number of positive cell lines: 5.  Mean: 3.603689745.  Mean(log): 2.101099999.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC063887</geneId>
<geneName>BC063887</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2054</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>aatgagggcaaggtctatgtctgtaaattcacattttatccTGTAACAGTAAGCATTTGGCTATTTGTTAGATTAATAAATGAATGAATGAAGATAAATAAGAGGAAGAAATTCTAATTAGTATTACCTAAGCAAGGTAAAAATGGAAAAATAGGTATATGAAAATCCTGTATAACCCAGGAGTCTAGAAAAGTTCTGTAAATAAGAAAGTTAACAGAAAGTCCTGCCCCAAGCCCAGTTACTAGAGTAAGAGGCATGACAGAATAAGCTGCCACCTTGAGCTTTTCCTTCCTGTCTCTCTTCAGGCAGTGCCAGCAGTTACCCCTGTGGACGAGGAGAGCTCAGACGGGGAGCCAGACCAGGAAGCTGTGCAGAGGTAATGTGACATCTGGCAGTGCTTGCAGAAGCCCCTGGGCAGGCTCCCCTGCAACCAGCGAAAGGTCACCTCTGCCCAAGGAGGTGGTAGAGTGCAGCTTCAAC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003489</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.41356674  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.21638067  HeLa: 1.009079117  HT1080: 0.253882431  MRC5: 0.961006615  JEG3: 0.3981989  U87: 0.927392265  G402: 0.594517319  HCT116: 0.608064141  CRL1690: 0.570202099  AGS: 0.524940355  Panc1: 0.363464141  HMCB: 0.698542719  MG63: 0.15036299  Snu-182: 0.978541961.  Number of positive cell lines: 0.  Mean: 0.534335764.  Mean(log): 0.589612552.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK122838</geneId>
<geneName>AK122838</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2055</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CAAATGAGCAACTGCATCAGAACCGTTCCTCTGAGGTTACTGTGCTGGACTGACCTGGGTATCAGTCTCTTCACAACCTGAGCTTCTGAAAAAGTCATGAAATACCTGGACCTGGGATTTTCTGTGATGGGAGAGAATTATTTTTGTGCAGAAAGACTGTATTGCTACTTGAAGAACATGGCTTTCTGAGGGGATCAGAAACATGTCCATTTCAGAAAACATTGAAAGCATAGGAATCAAATTTTAGGAGAAAATAGTACTTACTTGCTTCTACTTCAACCTGAAGTAGAAACAGAAATGACAAGTTATAAGGAAATGCTTCTCAACACAGCCTTCATGATCCCTGTTCCTGGATTGTGGCCCGCCAAATTCATTTGTTTTTTGTGTTGCTGAACCAAATACATGTTCGTGCTCATTTCATTAGCTCACTGCTGGGTCAAGCCTCAGGTAGAGTCTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003490</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0999 protein.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.511904762  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.398295335  HeLa: 0.61654993  HT1080: 0.93236559  MRC5: 0.888059455  JEG3: 0.561587536  U87: 1.08702517  G402: 1.054655963  HCT116: 1.075186977  CRL1690: 0.606710536  AGS: 0.651358574  Panc1: 0.88963639  HMCB: 1.164584755  MG63: 1.020063938  Snu-182: 1.170284592.  Number of positive cell lines: 0.  Mean: 0.847221638.  Mean(log): 0.865454624.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK022302</geneId>
<geneName>AK022302</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2056</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>agggaacttgttggaaacacaaattcttaggggcccatcctgacctactgaatcagagtttgaaacagaattatatagataggacccaggaatcttctgtttaacaagttctccagacttgtcctatgctcagtgcagtttgagaagcactgTTCTAGCTGGTATGTCGTCTGAGTATTCTCATTAGCTCTCATTACTTCTGGCTGGCTGGTGGCCTGGGCACTTGGTCACTCTGAGGTTCCTTTCTCTCCAGGGGCTGCATCTTCTTCCCAGTTTCAAGGCTTACCTTCCCGCAGTGCAATCTTTCAGCAGCAACCTGAGAACTGTTCCTCTCCTCCCAACGTGGCACTAACCTGCTTGGGTATGCAGCAGCCTGCTCAGTCACAGCAGGTCACCATCCAAGTCCAAGAGCCTGTTGACATGCTCAGCAACATGCCAGGCACAGCTGCAGGCTCCAGTGGGCGCGGCATCTCCATCAGCCCCAGTGCTGGTCAGATGCAGATG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003491</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0999 protein.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.408839779  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.50703912  HeLa: 2.169739838  HT1080: 2.539579283  MRC5: 1.15199757  JEG3: 2.570637081  U87: 1.95547235  G402: 2.128208774  HCT116: 1.849147569  CRL1690: 0.952321536  AGS: 2.153360791  Panc1: 1.731839153  HMCB: 1.505615538  MG63: 1.446453966  Snu-182: 1.155929671.  Number of positive cell lines: 3.  Mean: 2.822310535.  Mean(log): 1.844095874.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC035583</geneId>
<geneName>BC035583</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2057</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CCATCAGCTCCAGAGGTATGAGTCATTTTGTGTTGTGCCTAAGCCATTGTCTCGATAGCCTGGTACCCTTGGCTTGACTCACTGGGAGATATGGACTGACTTGAGCATTCATCTTGCAAGAATCTATTTGAAAAGGAGAGAAACCACTGTAAATTTCAGGAGCCTTCTTGAAATCCCAACTTCCTGTGCCACTTCATTTCCTTAGCCCCATGAGCAAAGTAATCTGATATCTAATACAGGAGCCAGACATAGGCCCACAATGAACTCTGCCATTTTGGCTGAGTTCTTTTCAAACAAGATGTAGATAGGTTTTAAATACACTGTGGTGGATGGCTTATGTATATTTTTCTAACATGAGGCTTATCAAAGTAAAAAAAAATAGTTTCCACTGATATATGTTGTATGGCTGAAACTTAAGATTGTACTGTCACCTTAGGAAGCTTCTTTGTGTATCTCTTTTGTTATTTTTAAGGTTAAGGATTCAGCCTTCAAGCCCACCCCCCAACCACCCCAACAACCATCTCTTCAGGCAGCCCAGTAATA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003492</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "CDNA FLJ25293 fis, clone STM07384".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.390852391  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.191859198  HeLa: 0.481230879  HT1080: 0.626506236  MRC5: 1.187111553  JEG3: 0.41081162  U87: 1.127491913  G402: 0.574256272  HCT116: 0.566686005  CRL1690: 0.637019512  AGS: 0.46823744  Panc1: 0.303774266  HMCB: 0.626419874  MG63: 0.321444885  Snu-182: 1.139868279.  Number of positive cell lines: 0.  Mean: 0.572358716.  Mean(log): 0.618765567.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK058022</geneId>
<geneName>AK058022</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2058</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ttcctaaccttaagcgatcctccctccttgacctccatgagccactgcgcccagccAGCaaacaatttttttaaaaaagcaaaacttaccttactatgtacagtgcatttcaatatattttattctattccattttaaaaaatgctgatttcgacttactaaattgatctcCTATCTGCTATTTCAGAAACAATGACATAGAAATACCTTTATAACCTGACTCCTGCCTAGCTCTTCAGCCCCAGCTCCCACTCTCCCACCAGTCACCCTAATTTTCTTCTCGTTCCCTGAACAAGTTCTGTTTTCTGGAGCATTTCCCACTGCCGAGAATACATCTTCCCTATCCCACCCCACTCCACCCACTCCTGTATTCTAGAATTCAGAATAAAAAAAATTAGATTGGATAGAAATAAGAATCTAGATAATTTCTATTCACTCTTCATGTCTCTAAACTTTCTCTTATCGTGGTGCTTACCAAGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003493</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.471349353  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.251623288  HeLa: 1.977960879  HT1080: 1.478933451  MRC5: 1.210251808  JEG3: 2.238482654  U87: 1.723764577  G402: 1.842043092  HCT116: 1.96287029  CRL1690: 0.93126922  AGS: 1.311046576  Panc1: 1.403862182  HMCB: 1.487066383  MG63: 2.023014737  Snu-182: 1.310042413.  Number of positive cell lines: 0.  Mean: 2.263537079.  Mean(log): 1.653730825.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>9681</geneId>
<geneName>DEPDC5</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2059</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ACTTCTGCCTTCCTCCTCTTTGTGGTTGCCTTGCTCAGGACATTGGCAGCAAAACGAGAATGGTGGGAGTGTCTCTTAAGTCTCGAgtgaccttgagcaagtcccttgcccggagtcacactttcatcatctacaaaatgagtgggctaacctcttttaagatctcttTACTATTTGGGTGTTATTGGTGTAGATGGAGACAAGGTGATGAGCACCCATTCAGCGCAATGCTTCCCCTATGGGGGTGTGATAGAATATCTTCTCCTAGGTTTGACTAGCCCCTGGCCCGAATTCCCCTTAGTTCCTGGATTCTGTGGTTCTATTTGTTCTCCATCGCTCCTTGTAACTGGAGGAGTGACTTCTTCCGAGAGTCACTTGGCACCACTTCACAGCAGAGGAACACCAGTATCTTCACTGGCCTAAAATCAAAGAGTGGTTGCAAGGAAAAATCTGACATTCCAACCTTTTCGTTTGTATTTCTGTGGCAGGGAGGCAAGATGACTTCTCTGCCCCAAGCTTGGAACAGCTAAAGGGAAAAACA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003494</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0645 gene product.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.698947368  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 7.912607423  HeLa: 7.560187359  HT1080: 7.800827867  MRC5: 5.135153871  JEG3: 8.561375119  U87: 7.057165596  G402: 4.826535451  HCT116: 6.363054941  CRL1690: 7.204575135  AGS: 8.578846881  Panc1: 4.716717661  HMCB: 8.54434633  MG63: 7.851041482  Snu-182: 4.383338075.  Number of positive cell lines: 14.  Mean: 176.9084046.  Mean(log): 6.892555228.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>9681</geneId>
<geneName>DEPDC5</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2060</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AGATCACTGAGTCGGAAACGAAGCTCTGTGGCCATGGATCTACTTCGGATAGACTAGGAGGAAATGGATTTCCTCCGTGGGGCGGGAGGCTCTAGTGCTCGAGGGCAGGAAACGCCAGGAGGTGGCCCAAGGAAGAGGCCGCACACGACGCCCCGCCCCCGGCTCGAGCCCCGGATGAGGAAGTGGTGCGGCCACCGAGACGAGACGGAGGCCCGGCGAGAGCGGCGCGGGGGCGCGAGGGCGGGAAGGAGGCGGGGCCCCGGGGCGGAGCCACCGGAGCGGCGCGGGTTCTCAGGTGAGCGCTACACGGTCGGGGCGGGCCTAGTAGGCGCTTCAGGCTTAGGGGCGGAACAGCGCGGGCCGCGCGGGCGTAGGCGGGGTATCTGGAGGAGGCGCAGGGAACCTGGAGAGGGTCCAGCCCTCAGTGCCCCGGCCAGAGGCGGGAAGGGGCTCTAGAGCTTCGGTGAGTGGAGCT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003495</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "CDNA FLJ41905 fis, clone PEBLM2006113".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.520912548  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.153719993  HeLa: 1.158402558  HT1080: 0.853140688  MRC5: 0.606383825  JEG3: 0.312066924  U87: 0.755351185  G402: 0.966115254  HCT116: 0.564835718  CRL1690: 0.424781476  AGS: 0.470712829  Panc1: 0.572279142  HMCB: 0.559026962  MG63: 0.389088796  Snu-182: 1.075717726.  Number of positive cell lines: 0.  Mean: 0.581526306.  Mean(log): 0.632973077.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK123899</geneId>
<geneName>AK123899</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2061</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ggcctcgtctctaccgctactattaataataaactagctgggcatagtggcatgtgcctgaaatctcagctactcggaaggctgaggtgggagaattgcttgagtccaggaagtcagctgcagtgagccaagatcgtgccactgcaccccagcctgggtgacagagtgagaccctgtttcaaaaataaaagaaagaaGGGGTGCCCAGGCCACAAAAGGGCATTTTGTGAGATGTGGGCACATTCCTGGCACATCTGTCTCCAGGGAGTTTACTAATTCCTGGGGAATAAGGAATGCCACTCTCTGGTGGAGAGGAAGAGACTCACAGAGAAAAACAGTTTATGAggccgtgtgcggtggctcacgcctgtaatcccagcactttgggaggccgaggcgggaggatcacctgaggtcaggagtttgagaccagcctggccaacatggggaaaccccatctctactaagaatacaaaaattagccaggtgtggtggctcatgcctgtaatcccagctactcgagagg</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003496</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.529296875  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.108801796  HeLa: 0.561781819  HT1080: 1.301165628  MRC5: 1.383799287  JEG3: 0.767617278  U87: 0.569766766  G402: 1.172518215  HCT116: 2.317103675  CRL1690: 1.181482947  AGS: 2.926505444  Panc1: 1.214037828  HMCB: 0.929888682  MG63: 0.625201349  Snu-182: 0.869080941.  Number of positive cell lines: 2.  Mean: 1.613953922.  Mean(log): 1.209196547.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>NM_015372</geneId>
<geneName>NM_015372</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2062</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>cgcccgaatttctgaatgtataggtctaaggcggagttcaagGGGATCCTCCCAGGTCTCAGGAGGTTGTACACTGAACATAGGTTGGTGGTCGCAGTTGTTCTACCACTGTGTGACCTTGACGCAGGGAGAGGAAATATTCATTTACAGAAAACGTAAAATAACGTGGAGAGAGAGTGAGATGGTAACCGGAACTCAGAAATGCAGGTGGTGTGTGACCCACGGTATTTTGCTAGGGTGTGGCTGGGCACGACTCATCCACCGGAGAAGCTGCAGAATCGATTTATGAGGGTCTCAGGAATGCAAAGACACACAGATTCGTCTCACCTAGAAGTCACGTTTCATTTTAATCTCCAAGCAGACAGCGCAGCAGCAAACCTGGGGCTGTGGAGTGGGGCCCCACACCCTCCGCCCACTCTCCCGCCCCCGTCCACGCCTAGACTGCAGGAAAGGGGTCTTCGCACACAAAGCCAGACCCCCAGGCGTGGGAAGATGGAACCAGAACAATTCGA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003497</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "solute carrier family 5 (sodium/glucose cotransporter), member 1".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.646365422  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.158083197  HeLa: 1.51955166  HT1080: 2.121386779  MRC5: 1.349398463  JEG3: 0.682896137  U87: 1.58526003  G402: 2.222850081  HCT116: 3.371821284  CRL1690: 1.170560581  AGS: 4.055416229  Panc1: 2.788334493  HMCB: 2.839622321  MG63: 1.357149497  Snu-182: 0.92679822.  Number of positive cell lines: 4.  Mean: 3.930773459.  Mean(log): 1.939223498.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6523</geneId>
<geneName>SLC5A1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2063</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GAAGAGTGCTGCACCCATTTTACAAGCGGACAAGCCAAGTCCTTAGAAGGCATGGGACTAGTCCAAGGATGGGTGGCAGGTGATCTGAAGCCTCTAGGCTCCTAGCCCCAGGTGGCCTGTTCCCTCAATGGAGCCACTCCAGCTCTGGCAAGGGCAGGTGTGGTGGCGCTGCTGGTGCCTGCTGTGGGAGTACAGTGGGCCTTTGTGCCAGGCGGGCACCACCCCCTGGCTGGCCCCTCCCCATTCGCAGGACAGCTCTTACCTGCCGGGCCGCCGCCCCAGCCAACAGCTCAGCCGGGTGCTCCTTCCTGGGCTCCACGCCCGGAGCTGCTTCCTGACGGTGCAGCCGCAAGGCATCGCAGGGGCCCCGCGCTACTGCCCTGCTCCCTCAAAGTCCCAGGTCCCCTCCCCTGGTGCTGATCATTAACCAGGAGGCCGTATAAGGAGCTAGCGGCCCTGGCGAGAGGGAAGGACGCAACGCTGCCACCATGGACAGTAGCACCTGGAGC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003498</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: hypothetical protein LOC150297.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.503636364  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.370986483  HeLa: 3.267156962  HT1080: 5.014079932  MRC5: 2.424264871  JEG3: 2.298441794  U87: 3.684310503  G402: 4.067885513  HCT116: 3.708685057  CRL1690: 2.186543523  AGS: 3.405897455  Panc1: 4.520662823  HMCB: 4.199373489  MG63: 4.273613371  Snu-182: 1.263497521.  Number of positive cell lines: 11.  Mean: 11.73717525.  Mean(log): 3.334671378.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC040263</geneId>
<geneName>BC040263</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2064</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CAGTCATCACGCTTTATCGAGAGTGGGACCAGGGCTCTAGGAGTTGCTGTGGTCAAGTTGAAGACAAAAAGTAACACTTGTAAGACAGGAGAGAAGCATTTACTTACAAAGCAGTCCGAAATTTGTGTATAACTACATTTGGTGAGCAAACGAAAGCTGCCAGACTCAGAAAAACAGAGATGCTAATGGAACTGACTTTAGTAACCAGGGTTTTCTATTGAGTTCATTGCCCAGGGTGACTTCCAATAACAACCTCCAACCCCTGCACTTTTCTCAGGACTGGAAAGCTCAGGCAGCCCAGGATGAATAATGCAGTCACCACAGAGGGACAGGGTGGCCACAAGGTGGGCAGCAGCAGGGATGGGCATTGTGAGGCATTTGGTGGGTCTGTGGGGTCGGCCATTGTGAGCCACTAGCCTGACTTGGTTGTTTCCTGGCAACCAGGTGACATAGGAGGTTTTGTGGTTACTAGGCAACGGCCAGGGCCAGCAGCCTTCAGTCGGTAGCTGGCCGTAGAAGGAGGAGGAGCTCCGACTACATTCTGTCCTTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003499</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: ret finger protein-like 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.646271511  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.262584339  HeLa: 1.638160126  HT1080: 1.288915702  MRC5: 1.031169292  JEG3: 0.264606395  U87: 1.543834129  G402: 1.378289571  HCT116: 1.297363925  CRL1690: 1.062663732  AGS: 1.691652597  Panc1: 1.564910765  HMCB: 1.213081253  MG63: 0.954430916  Snu-182: 0.755420729.  Number of positive cell lines: 0.  Mean: 1.299694566.  Mean(log): 1.139077391.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>10739</geneId>
<geneName>RFPL2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2065</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>gtaaggagcagtagtgcgtgttgcattgctcatggcgggggagggttgggtgcgttatcccgggcgtcatttcccacagcggcgggggtcagtggaggggcttgttgagggcgctatccatggctgcactggtcgctgaggggcaaggattgggggcgctacctgggacatcagtgccatggtggggaacttgttgggtgtgttatccgaggcatcactccccatggctgggggctggttgggggcgctacccatgggctgcactgcccacagccaggagcgtgtatgggacattatcgggggcggactgccagtggctgggtggggaggcgggttggatgctatgtggggttgcactgcccagcagggagtgagttcggtgcgctatctggggttgcactgccggcggtgggtggcagattgggtgccctatcgctacactgccgcggcgagtaccgggttggcggcgctatcctgggctacaccgccggtggcgggaggcgttttaggggcgctatctggt</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003500</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: ret finger protein-like 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.509846827  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.231683069  HeLa: 3.458496248  HT1080: 2.889370626  MRC5: 1.747180907  JEG3: 1.921554557  U87: 2.783065356  G402: 2.141334964  HCT116: 2.350195112  CRL1690: 1.452745678  AGS: 2.423396038  Panc1: 2.729424787  HMCB: 1.669165916  MG63: 2.699344938  Snu-182: 1.393100055.  Number of positive cell lines: 8.  Mean: 4.094654676.  Mean(log): 2.206432732.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>10739</geneId>
<geneName>RFPL2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2066</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>gcggtagatgactctagcctctggcatgcgcggcaagtggctcctcctccttctcctctaagccgggcacagagcagctacgcaggccgacgcagatgagcctggaagggcaagccacccctcttggcatcctttatatactgagtttaatgcaaatgaagtttctcgactacatagtctgatcggatgagagaaacctctaggcctactctgatcgggctttgttatcttgttctgattggttatcctaagacttgctgtcatccagtcagaacgtgaaaataaagcacaatcagagtagacctagaggtttttctctcatccaatctgaacatgtagtccagaaaccttacttgcataacctcggtctgtggggggaggggttcttgccattccaggcacttctgcgtctgccagcccatctgctccatgcccaggttagaggaggagtcacctg</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003501</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "solute carrier family 5 (low affinity glucose cotransporter), member 4".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.514925373  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.117205449  HeLa: 0.628090888  HT1080: 0.258557009  MRC5: 0.885409318  JEG3: 0.305180313  U87: 0.454317484  G402: 0.409038824  HCT116: 0.414075938  CRL1690: 0.904150756  AGS: 0.26894775  Panc1: 0.33095626  HMCB: 0.53068012  MG63: 0.355838124  Snu-182: 0.672252056.  Number of positive cell lines: 0.  Mean: 0.399413531.  Mean(log): 0.466764306.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>6527</geneId>
<geneName>SLC5A4</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2067</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GAATCCACGAAAGGCATAATTCACTTCACTGTCAAGGGATATAGCTCATTGGTCAGAAACTGTATCTGTTCTCTGAAGGACCATTGCATTCGGTCCCTCCTGGCTGGTTTCTGGTACCTTCTAGTCTGTCCTTCTCCCCTCCTTGTCTGTCTTCATTTCTCTCAAATCCCCCCTCCACCTGGGCAAATCTCTTTAAAGACCCTGTCTTTGCACTCAGAGAACGCCCCATGCTCCACCTCAAATTCTCCCCTCATTTCTGGCCCTGCATCCCTCATTCTCACACTCTACCTAGGCTAGCACTCACTGGTGGAGGGCTGGGGTGCCACAGCTTTGGAGAAGAGGTTTAAAGGTCTCCATATCCAGGAGCTGGCTCTGATATCTCGCCCCACCTGCCTGAGGCTGATCATTAACCCAGAACTTATATAAAGATGGCTCATGCGTGGAATGGGTATAGCACTGCCTGCAGCCATGGCCAGTACGGTTAGCCCCAGCACCATAGCTGAGACCCCAGAGCCACCTCCATTGTCTGACCACAT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003502</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: developmentally regulated GTP binding protein 1.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.5  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.584199094  HeLa: 1.266524277  HT1080: 0.892828451  MRC5: 0.913482044  JEG3: 1.242088597  U87: 0.735522547  G402: 1.000992793  HCT116: 1.003591203  CRL1690: 0.760497216  AGS: 1.036538414  Panc1: 1.153221044  HMCB: 1.101775167  MG63: 1.4591828  Snu-182: 1.15086549.  Number of positive cell lines: 0.  Mean: 1.161932111.  Mean(log): 1.092950653.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK055495</geneId>
<geneName>AK055495</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2068</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TCATCAGTGTTGGGTTGAATGTTGAGCTGAACTATGTTGCCACCTGGGCCACTAAAATGCTTttttctttttctttttctttttttttttttgagatggagtttcgctcttgctgcccaggctggagtgcaatggcatgatctcggctcaccgcaacctccgcctcccgggttcaagcgattctcctgtgtcagcctcctgattagctgggattacaggcaggtaccaccatgccccgctaattttgtatttttagtagagatggggtttctccatgttggtcaggctggtcttgaattcctgacctcaggtgatccgcctgcctcagcctcccagagtgctgggattacaggtgtgagccaccgtgcccggccAACTAAATGCCTTCTTTCCCATAACCCAGACTTTCTGCTTGAATCCCCATGAAAGTCCTGGCTTCAGCCAATAACTTGGGCGAAGGTGCATTGCAAGTGAGGCAACTGGTGTGATCAAAG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003503</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: developmentally regulated GTP binding protein 1.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.445564516  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.089778949  HeLa: 0.260044186  HT1080: 0.304355632  MRC5: 0.861794328  JEG3: 0.318870345  U87: 0.441353434  G402: 0.805988525  HCT116: 1.089941124  CRL1690: 0.684865815  AGS: 0.583497435  Panc1: 0.163043084  HMCB: 0.446870653  MG63: 0.213089679  Snu-182: 0.897907018.  Number of positive cell lines: 0.  Mean: 0.457671425.  Mean(log): 0.511528586.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK074476</geneId>
<geneName>AK074476</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2069</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTTCATTGAGCAAGCATTTAGCACTGCCAGAATGTTGGGGAGAGAAGGTTGCTGAAATCCAGTTCATCCTAAGGCCTCAGGATGTTCTGTGAATAGGCTTTGTGTCCATCATTTAGCACCCTCCCCATGGCTTGGTCCAGGGACCCCTGGTCTCCTTGAGGAGAGAATTACCCTACCTTTCCCTTTCTCCTCTGGGCTTAGACTTAGCAGTTCTGGGAGAGGGGTATGTTTGGTATTGGGAATGCTGCCTAGGGTATGGCCACTGTGGAGGTACAGCTAAAGGCTTTCTCCTCATTAACTCTAAGACTTTACTGGTTTGGCTGTCATAGCATGATTTGAATTTCCTGTGCTTTTACATATTCCATGTTTCTTTCCTGACTTTATTACAAGTAAACAGATCCATTGTTCTGTGCCATTTAACTAGTTAGAACACGTTTAGCTGCATTTAGCAGAAAGTGCTAACTTAAGCGGCTGAAATGGAAGGGAACTTGGTCTT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003504</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: developmentally regulated GTP binding protein 1.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.429400387  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.081653158  HeLa: 0.72785813  HT1080: 0.258331367  MRC5: 1.08066876  JEG3: 0.245109157  U87: 0.893275342  G402: 0.380222058  HCT116: 0.508201416  CRL1690: 1.034720001  AGS: 0.257205058  Panc1: 0.456443595  HMCB: 0.545846738  MG63: 0.628929961  Snu-182: 0.8482066.  Number of positive cell lines: 0.  Mean: 0.51532116.  Mean(log): 0.567619382.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK127132</geneId>
<geneName>AK127132</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2070</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGGTGTCACCTTGTATGTCGAACTGCATAAAAGATCTGGTAGGCTGGTCAGCTACATGCAGCTCATGTGTCATTGTCAGAATTTGTTTTGGGATGGGCTGAATGAGGAAGGGTATATACGGTGAAGCAGCTACAGAAGGGATCCTTGGGAACTTCATCTTGAGTGTGAAATGGATAAAAATATGACATGCTGCATCTTACTTGATGTTTACTTATGGGAACCCCTTCCAAACTAGATATGGCTTTCAGTCCTTTCAAGTAGTCTTTCCCACATGATACTGGAGAGAGGAAGGACTTTATGTAAGTTAATTGATCACTCCCCGCAAGGCTAACCTATTTTGGGAGATCATgtaattaagtactccgaccaggcagatcagggtttgaaattgcaggtccacctctagttagctgtggagccctgaacaaattacccaacctttatgagcctcagtttcctcatgtaacatggggatagtaatagcacttactttctgcggtggtgattgttagtaatg</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003505</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "CDNA FLJ36925 fis, clone BRACE2005169".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.438563327  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.046314501  HeLa: 0.491209088  HT1080: 0.278578493  MRC5: 0.635977852  JEG3: 0.233820299  U87: 0.463411167  G402: 0.346866265  HCT116: 0.392888041  CRL1690: 0.303246673  AGS: 0.195677744  Panc1: 0.135761547  HMCB: 0.326904909  MG63: 0.357494323  Snu-182: 1.002943431.  Number of positive cell lines: 0.  Mean: 0.311589192.  Mean(log): 0.372221024.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK094244</geneId>
<geneName>AK094244</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2071</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGCTCGTAATCTTAGAAGTCCGCAGAAGGGGGCTTTGGGCACAGGCAGCATTCCCTTCTCTACCACCTCGGCTGTCCCTGGCATCTCTGTAGAAGTTGTCCTTCTCGGAGGCTGCACTGGGTATTTCAGATCTCATCTCCCCCATCCTGAGGCACAGCAAAAGGGTTTTCTGGAGGAAATACAAGGAAAAAAAATATCACATGGTGTCTCCTCAATGGGGACTCACTGGGGACATTTCTCTCTGGCCTCAGTGCCAGAAGAATCCAGGTTTCCTCTGAACACATGGGTTTTGTCTTCTGAACGTTGTGAACCATGTGActttaagactggaagcgagacaaaaatgtcgctatcattatagctccatatagtactagagctctggctcatgcaataaggcaagaaaaaaaagcatagactaggactggaatagaagaaccaaaattacagttaattgtggataacttacatagaaaatttaatagaatcaacaggttaattagtagaaTGGAGAGTGCATACATAGAGG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003506</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: ret finger protein-like 3.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.545454545  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.122496024  HeLa: 0.419920421  HT1080: 0.458664002  MRC5: 0.986548315  JEG3: 0.222455752  U87: 0.651749811  G402: 0.618916578  HCT116: 0.708242879  CRL1690: 1.053084938  AGS: 0.891045217  Panc1: 0.56861221  HMCB: 0.667463307  MG63: 0.722003213  Snu-182: 0.794547561.  Number of positive cell lines: 0.  Mean: 0.576740144.  Mean(log): 0.634696445.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>10738</geneId>
<geneName>RFPL3</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2072</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>gagatggtgtctcactctgttgcccaggccggagtgcaatggcacaatcttggctcagtgcaacttctgcctcccaggttcaagcgattctcctgccaaagcctcccaagtatctgggattacaggcgtgtgccaccacgcctggctaattcttttgtattttcagtagagatggggtttcacccatcaggctggtctcgaacttttgatgacctcagatgatccacccaccttggcctcccgaagtgctgggattacaggcatgagccatcgtgcccagccTCTCAGCTCCTAATTCTTATGTTCATCAATCAGTCTCTTGCTGGGGTTCCCCTAGGAGGTGGTGAAATGACCCCAGCTCGCTGTTCCTCACATGGGTGCTGCCACGTCACTGGCTCAGGCTCAGCTGCTGGGTCACCAGGAGAATGGACCCTTCCTCCACCTCAGCTCAGAGCACAGTGATGATTCGTGAC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003507</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: ret finger protein-like 3.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.62992126  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.151429836  HeLa: 1.376110135  HT1080: 1.773526249  MRC5: 1.100587627  JEG3: 0.498701655  U87: 0.815822193  G402: 1.060610615  HCT116: 0.855471559  CRL1690: 1.265087333  AGS: 1.056570729  Panc1: 1.461498118  HMCB: 1.365174452  MG63: 1.441705211  Snu-182: 1.167443531.  Number of positive cell lines: 0.  Mean: 1.301763878.  Mean(log): 1.17069566.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>10738</geneId>
<geneName>RFPL3</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2073</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>aatgatgccctggatataacacgtcccgcccaccgcaggcagagtagcacccgatagcgcccccaacccgtgcctgacaagggcaatgcaacacccgatagttcttccaactcgcccgccggccacggccactgcatccccagatagtgcccccagaactccccactgccgctagcagtacagcttgggatagtgctccaacccacccccagccacgggcagcgcacacccgatagcacccccaacccactcccctctgtgggcagtgaggccccagataccacatccaaccagcctcctaacacgggcagtaacgccctggatagggcctccaacccaccccaccacgccacgccacaggcagtacggcctgggatggcgaacttttcccaccaccattttaccattctggctgcgctctagtctccctggcccgcaccaacggcagcagcgaggtgagccacggcaggctccagcctccactgtgctaatgaagttgctcctcctc</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003508</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:5272895, mRNA".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.499061914  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 4.575044027  HeLa: 2.891896318  HT1080: 2.968380988  MRC5: 1.402560223  JEG3: 4.406322659  U87: 2.53674797  G402: 2.042405215  HCT116: 2.590623921  CRL1690: 2.613233582  AGS: 3.188027915  Panc1: 2.37205639  HMCB: 2.939852674  MG63: 3.239638252  Snu-182: 1.666418146.  Number of positive cell lines: 11.  Mean: 7.541512697.  Mean(log): 2.816657734.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>10737</geneId>
<geneName>RFPL3S</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2074</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>tgagcttgggttttgttgttttttttttaagtaaaacgcctaatcttttattttattttattttattttattttTTTacggagtctcgctctgtcgcccaggctggagtgcagtggcgctatgtcggctcactgcaagctccgcctcccgggttcacgccattctcctgcgtcagcctcccgagtagctgggggctcccgccaccacgcccggctaattttttgtgtttttagtacagacggggtttcaccatgttagccaggatggtctctatctcctgacctcgtgatccacccacctcggcctcccaaagtgctgggattacaggtgtgagccaccactccctgccgtaaaaggcctaatctttaatgaccctcctgtgcgtgtgaaagcactcttgttggtgcagcagaaagcggacctcacaatacacattgtgactttaccctgagacgttgatgatgctcctatcaccatggttatgtgattgggtatatcttgccctcggtcctaactgccactgtctgtgctga</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003509</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Hypothetical protein LOC339666, mRNA (cDNA clone IMAGE:5272406), partial cds".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.573012939  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.265496675  HeLa: 1.650350312  HT1080: 0.909671675  MRC5: 0.941351172  JEG3: 0.475716061  U87: 1.03614205  G402: 1.041270019  HCT116: 0.801698729  CRL1690: 1.123197562  AGS: 1.089250561  Panc1: 0.826487791  HMCB: 0.678968657  MG63: 1.06845802  Snu-182: 1.133692923.  Number of positive cell lines: 0.  Mean: 0.953878578.  Mean(log): 0.931553729.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC041349</geneId>
<geneName>BC041349</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2075</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TTCTTTTAGTATCAGCAACTTGGGCCATGGCCCAGGGCGTGGCCATAGATACTTCTAGACTGACACTCACTAGGCTCTCAGGCCGACACCACTCACATGACTTCTACTGAGGGAATGCAGTCTGGCGAGAGAGCAGCAGGAGACACTGTGGATCTCAGGGTCTGTGCAGTGGGCAGCCACAACTGTGCCAACCCCCTCCTACCCCACAAATTCCGCAGGGCTGGGTGATGGAGCCTGCACTCACTGAGGCTGACCTGGAAGCTGTGCCCTCCCTGGGTGTGGTTCCAGCACCCACTTCTTCCCAGGTCTGGCCTGTCGGACTTCCCCTGTCCACCAGCCCCTAGGACTTGAATAAATACATGGGGTAAAGTAGAGGCAGGCAATGTGGGGACACATTGGCATCTGTAACTCCTCCTCTGTGAGGTCAGTGGAAGGGATAAGAGAGGCCTGGAGCAGCCCACTCCAGCTCTGGACCTCAGAAGGGCTGTGTCCACCATGGCTCCTGTCCTCCTGCTGCTCCTCTCTCACTTCCCAGGTAAGG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003510</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.594059406  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.35843741  HeLa: 1.011325049  HT1080: 2.618786376  MRC5: 1.31904034  JEG3: 0.910833222  U87: 1.456397071  G402: 1.392557937  HCT116: 1.640169068  CRL1690: 1.17199185  AGS: 1.17165472  Panc1: 2.637952232  HMCB: 1.757334498  MG63: 1.427181371  Snu-182: 1.012860512.  Number of positive cell lines: 2.  Mean: 2.21187858.  Mean(log): 1.563322975.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AL110165</geneId>
<geneName>AL110165</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2076</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GCACCTTAGGTCCCCAGTAAAATATAGGGGAGGCTATGGCCAGGGCCGACCCCCAAGAGAACCATTCCCAGCACAGGGGTTTCCTATCTCTGCCTGTCCTCCATGCCACATCTGCCTCTCCCAACCCAAGCACCAAGTGGCCCAGAGCTGGAGTTTTGATGGGCAACCTGCTCACACATCTGCCTGGAGCTGCAGTTGTGAGTGCCCAGGTGCTCAGCACTGTGTGCCAGGGCCTTTGGGAAGAGAATGTCAGTAGGAAGCCGGGGCCCGCAAGGGTCTGTATAGCCCTGCTGCATGGCCAGGTCTGCCCCTATCAAGACAGCACAGATGGCTGGGGCTGGAGTGGGGCTGTCCTCTACACAGGAAGCAACAAGCCAGGGGCCCAGAACCACAATAAAAAGCCCCGCAAGggccaggcgcggtggctcacgcctgtaatcccagcactttgggaggctgaggcgggcgaatcacgaggtcaggagatcaagaccatcctggctaa</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003511</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: hypothetical protein HSPC117.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.453358209  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 9.488552084  HeLa: 8.728497537  HT1080: 9.340221071  MRC5: 7.441315106  JEG3: 8.179137967  U87: 9.911413556  G402: 5.684594804  HCT116: 6.987834821  CRL1690: 9.023240058  AGS: 9.015807029  Panc1: 5.377281549  HMCB: 10.15566564  MG63: 7.747052785  Snu-182: 4.860657266.  Number of positive cell lines: 14.  Mean: 417.556052.  Mean(log): 7.995805091.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AF161466</geneId>
<geneName>AF161466</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2077</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GATAAGCTGCCATGCTTCATTCTTTGGGATGCTCCTTTCTGACCAAAAAAGTTATTTGGTGTATATCCAGATTCATTCTGAAACATAAATGTTCAGCTATGGTATTTACTCAAACAGGTTTTTCTTTCTCAGCTGCTGGCGTTATCTTTTTCCCCTCCCAGCTGAGGGTGTAAACTCCAAGCCAATGCACCGAACCTGACCCAGACTCAAGGTGTTTTCATAAGCTGCTGAAAAGCATTTCCAAAACAAAAGATAACTAGATTATACTTTAAACTTCTGGATTTCGCTTAGCTGTAGTTTAGAGGAAATCGACTAATAAAGATCCTAAAGTTATACACTACAGGACAGTACAACTTAACCAGAGGAAAGACATTGGCCTGAAGAATTTTGAGCCTCGGCGCTTGCCGTTGCTCATCTGCTGCGGCGCTGGTCGCGCCTGCGCTTTGGTTCTTGGAAGGCGGTGCTCTGAGAAGCCGGACTACGCGGCAGCGGCTCTTCAAAGCGGAGCCGGGAGTTTTTGCTACAGTTTTCGCCAC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003512</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: bactericidal/permeability-increasing protein-like 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.432926829  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 1.255099713  HeLa: 1.412965396  HT1080: 0.490930533  MRC5: 0.904610308  JEG3: 1.148283998  U87: 0.716888686  G402: 0.959222118  HCT116: 0.921030459  CRL1690: 0.673829843  AGS: 0.777030467  Panc1: 0.623067365  HMCB: 0.989166677  MG63: 0.666282679  Snu-182: 1.112757773.  Number of positive cell lines: 0.  Mean: 0.900612886.  Mean(log): 0.903654715.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>254240</geneId>
<geneName>BPIL2</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2078</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TGAGGGAAGTTTTCACAGAGAGGGACATGGAGCTGGCCCTGAAGGATGCATAttcactactagtctgtgaaaaacataggtcaggggccatgtgtaggtcaacactacacccttagcacctagaacacatgctggtgtgttcaataaatgattgCtgaatgaatggatggatgggtgggagagcgcatggatggatggatggatggatggatggatggatggatggacggatggatggttggatggatggatggatggatggatgaatggatggattggatggatgTATTGAGTTCTGGAAGTAAACAGTAAAAATGAGAAAATCTAGAAATGTTGGATTTAATTGACCAAAGAGAAAGTCAAGAATAATAAAGGAACCTTAACTGTTGGTTAATTTCAGATGTGTACAAAGACAATCCCAGTCCTCTGGGGATGTTTCCTCCTGTGGAATCTCTATGTCTCATCCTCTCAGACCATTTACCCTGGAATCAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003513</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: bactericidal/permeability-increasing protein-like 2.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.43071161  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.890057551  HeLa: 2.215322918  HT1080: 2.35853875  MRC5: 0.96928399  JEG3: 3.66762625  U87: 5.710325091  G402: 0.832694388  HCT116: 2.822709488  CRL1690: 1.383796193  AGS: 2.225432754  Panc1: 1.026190194  HMCB: 0.453482059  MG63: 1.161495869  Snu-182: 1.219788393.  Number of positive cell lines: 4.  Mean: 6.340187469.  Mean(log): 1.924053135.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC062656</geneId>
<geneName>BC062656</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2079</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ACTGAGAGATGCCAACTGAGGTCCTACCCTGAGTGATAAGGTAACTAGGTCAGCCCGATTGTCAAGCCTCATGCTTTCAGACTGAATCTGATGATCCACCACAAGTCCCAAAGGTATTCTGGGCAGTAGTAGAGCCATCCACCGCAGGCACCCTGACCAGAAGGAACCAGCTTATGATTCCAGACAGGAAAATTCTTCCTCTTCCAATGCAGTTTAACACCGTTTTCAATCATTTTGGTAAAGTAGCCATCACAATTTCACAAGTGgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtTTTGCAGGAAGATAATTATTGCATAGGTGGCACTGTCTGTTTATCTAGGTAGATACTGTAGTGCTCATTCATGCCATTGGGTAATTGTAGTGAAGCAATTATGTATCACATTTTGAAAGAGGCATTAAAAAAATTCACCACTGAGATGAGTCAGACTTAATTATCTTGGCTTTTTAGCAGCTGAGTTTAAGGCGCAAGGTGGAGAACACATCAGCTTCAAAGGCAGAGAGAA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003514</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: F-box only protein 7.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.612244898  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 3.407662363  HeLa: 2.870178295  HT1080: 3.308184177  MRC5: 2.339777355  JEG3: 1.195396641  U87: 1.757297595  G402: 3.16593745  HCT116: 2.558206311  CRL1690: 1.924570078  AGS: 2.665858855  Panc1: 3.138486367  HMCB: 2.916087654  MG63: 1.912133756  Snu-182: 1.236952588.  Number of positive cell lines: 9.  Mean: 5.145985463.  Mean(log): 2.456909249.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>25793</geneId>
<geneName>FBXO7</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2080</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>caactagctgggactacaggcaggcgccaccacacctaattttttgtattttttgtagagatgggggggggggtttcaccatgttgcccaggctggtctcgaactcctgggctcaaacgatccacccgcctcggcctcccaaagtgctgggattacaggcgtgagccaccgcgcccggccAACCTAAGGATTAACCTAAGGCTTCTCAGAGCAGATGCCGCTGGAACTGAGGGCCACGGAAGAAAGGGGGTGACACTTGGTCCTGGGGAGTGGCGACTGTATTGTCTGTCTGCAGCATCCCTATCAGCGCTACCGTTGTTCCACGCACACAGGGAGTAAGTACTGGGAGTCCCAGCCACCGCCGCGGAAAATCTGGGATGCCAGCGAGCGGCCGCATCTCGGCGCCTGCGCACTGTGCCCGCGCTCTCAGGCAGCGCCGTTGCGCGCGGAGTCATCGATCGGCCGACCCCGAGAGGCCCGGTTCCTTTAG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003515</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: eukaryotic translation initiation factor 4E nuclear import factor 1.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.459558824  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 3.673909392  HeLa: 3.168399652  HT1080: 2.959286424  MRC5: 1.552595097  JEG3: 3.6024494  U87: 1.706287949  G402: 2.946430431  HCT116: 3.664340321  CRL1690: 1.236711354  AGS: 2.614373985  Panc1: 2.706721302  HMCB: 2.473607724  MG63: 3.967464792  Snu-182: 1.186191628.  Number of positive cell lines: 11.  Mean: 6.624478978.  Mean(log): 2.675626389.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>56478</geneId>
<geneName>EIF4ENIF1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2081</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TCTGGATAACCCTACAACTCCCAAGTTCCTGTACCTATTCTGTCTACCTGAACTGTTGTTCTCTAGCTTCTTCTTGATCGCACCCAATGGAATGCAGCTTCTTCCCCAGGAAGCATCCCTGCAGTGCCTTGTTATTTCTTCTAACCCCTCCATTTTCCCATTGTACTTTGTTGGTGCCTAATATCTACATGCCTTGGTTTGCTCTAGGTGATtgtctcccccgctagactgagagctcttacaagactgggactgtgtttcattttccttttgtcttccctcagagcttagcatgtgcttTTGTGTATGTTAGGCCTAAATGCTTGGGAAATTGAATTGGATAAGGGAAAGGGGATGTTAAAACTTCTAGGCTGGTCTTGAGTATTATATGGTTTTAAGACTTGAAGTTAAGCAGATTGGGGTTCATGCTGATAATTGGTTTGTTCACAGGCAACAGCGAGTGACCAAGTCACCAGCACCCGTGCATCGAGGGAATTCCTCTTCCCCTGCCCCTGCTGCCTCCATCACAAGCATGGTCAGTGAC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003516</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: eukaryotic translation initiation factor 4E nuclear import factor 1.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.387308534  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.875567858  HeLa: 1.373672858  HT1080: 0.355280004  MRC5: 0.984995729  JEG3: 0.887195339  U87: 0.714386651  G402: 0.65273188  HCT116: 1.025881808  CRL1690: 1.09033149  AGS: 1.363811209  Panc1: 0.510293652  HMCB: 0.742883268  MG63: 1.041443208  Snu-182: 1.26721014.  Number of positive cell lines: 0.  Mean: 0.93208891.  Mean(log): 0.920406078.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>486366</geneId>
<geneName>LOC486366</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2082</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>cagagcgagactctgtctcaaaaaaaaaaaaaaaaaagtaataaaaaaTAAAAAAGGAAAGTAAGTAGATGGTTATACTCAAGTTTGGGTTATTCAGAAATTACCCAGGATGGAGGAAGAAAAAGGTGTTCAAATTCCTAGGTTCTGAGAGTATTTATCTTCAGGTCACGAGCATGAAAGGAAGTTTCAAAGTAAGTGACCCTTTCATAAGATTTAAACCTTCTTGTCCTTTTTCATCTAGAAACTATTAGTTTTTATTGTCTTTTTCTTCAGATGATAGAAGATGTTTTGGGAGAAGGGTCAGTCTCTGCCAGTCGGTTCAGTAGGTGGTTCTCTAACCCGAGCAGATCAGGAAGCCGATCCAGCAGTCTTGGGTCAACACCACATGAAGAGCTAGAGAGACTTGCAGGTAAAATGGCTTCAGATTCTGCCCTTGAAGGTAAACCTGGGTTTTTCC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003517</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: eukaryotic translation initiation factor 4E nuclear import factor 1.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.446  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.265342438  HeLa: 1.066562758  HT1080: 0.838071542  MRC5: 1.19248212  JEG3: 0.454169115  U87: 1.173663879  G402: 0.998697883  HCT116: 1.200644159  CRL1690: 0.755651382  AGS: 0.610350843  Panc1: 0.976949747  HMCB: 0.717811355  MG63: 1.180738294  Snu-182: 1.028455781.  Number of positive cell lines: 0.  Mean: 0.887621456.  Mean(log): 0.889970807.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK130061</geneId>
<geneName>AK130061</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2083</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>cagcctggagaacatagacctgtcccaaaaaaaaaaaaaaaaGTAACCACTACTGCTTTAAGAGTGGAGGATTTGAATTTTGCCCTGTATGTGATACCCATTTTGGAACAGCTCGTTTAAAAAATAATAAAGTTgccgggtgcggtggctcatgcctgtaatcccagtactttgggaggccgaggcgggcagatcacgaggtcaggagatcgagaccatcctggccaacatggtgaaaccccgtctctactgaaaaaaaaaaaaaattagctgggcgtggtggcatgtgcctgtagtcccagttactcaggaggctgaggcaggagaattgcttgaaccctggaggcagaggttgcagtgagccaagatcgtgccattgcactctagcctggtgacagagcaagactctgtctcaaaaaataaaataataaaGCTTAAATTTCCTGAAATATGAAACTCTGAAATATAACAATTTTGGCCAAACCTGCATGTTGTTTACT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003518</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:4818531, mRNA".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.481262327  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.379549663  HeLa: 1.082157113  HT1080: 0.820509927  MRC5: 1.063814374  JEG3: 0.534380036  U87: 1.903869586  G402: 1.206738234  HCT116: 1.125531434  CRL1690: 0.862211656  AGS: 0.752349837  Panc1: 2.592528931  HMCB: 1.152318134  MG63: 1.109869829  Snu-182: 0.923919806.  Number of positive cell lines: 2.  Mean: 1.340514496.  Mean(log): 1.107839183.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK123891</geneId>
<geneName>AK123891</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2084</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GAGGGAGGTAAAAATGGAAGTGGCTTTGGCCTGGAGCAGCTTCTAGTTATGCCCAAGCAATGTAGATTGTTTGGTAATCAGCCAAGATCCATCCAGGTTCCCAGGAGCATAAAAGCAATCATCTCCTTTTTGGTCCTTCAAAACCAAACTGGAGTGGTGACGTCAGGGCCAGAGACCCTCTCCTTCTGTGGGCATTGGATCACTTAGAACTCTCAACCTCAGAAAAGCCTGCCTTCAAGCTGGCTTTTGACGGGCTATTGGCTGGAGACTGGGTCAGTATTGAAAGTGCTAGCTGTGCACCTGGCTGCCAGAAAGCCACTTGGCCTTTAGGACAGTCCTCTTCACATTGCCCTCTTCCCTCACTCATGATCAGGTCTGGATTTAAGAGCAAGAGACCCCAGGATAATTCAGAAGTCCTCTCTCTCCTCCTGTTCAAGACTCTTGGTCTGGGATTCAATAATAAGTAGCAGACCTGACATAAGAAAGATCAGATAGGTCCAATTGCCA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003519</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "Clone IMAGE:4818531, mRNA".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.512295082  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.301635954  HeLa: 1.482634327  HT1080: Bad Txfn  MRC5: 0.915261229  JEG3: 0.703129244  U87: Bad Txfn  G402: Bad Txfn  HCT116: 0.837409612  CRL1690: 3.128384408  AGS: 0.620371193  Panc1: 0.664562293  HMCB: 1.061488984  MG63: 0.893040555  Snu-182: 0.741162873.  Number of positive cell lines: 1.  Mean: 1.437319183.  Mean(log): 1.031734606.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>BC042456</geneId>
<geneName>BC042456</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2085</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ggtggaatgtcatcagttaaggcagggcagggtcttttcacttcttttgtgattcttcagttacttcaggccatctgggcgtatacgtgcaagtcacaggggatgcgatggcttggcttgggctcagaggcctgacaGCCCCCAAGAAGGTGAGGTGACTACAGGGCTGTGAGCTGTAGGGGAGATGCCATTGTCAGCATCGGTCAGGGAGGTTGGAGTGAGCAGACCAGGACAACTCCACAGCTTAAGCAGCAAAGGTCTGGGACCAAGGAAAGGAAGCACACAGACTGTGCTTCACACAACAAACACAGCAGAGTTCCAAACAGCACAGCCTCAGCTCGAACCAGCCCAGGAGCACACAGTGTCCTTTCAGGTTCTGCCCCTTCCAGCCCCTGAGGGCAGACTAATCTCTTATGCTTTATTCAACTTTGTAAAACACTGGTGGCTCATTTTATGTGTTTTGAATTGGTGAAAGGATGCAGGTTAGT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003520</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: synapsin III.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.464052288  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 2.108763543  HeLa: 0.696833342  HT1080: 1.602000032  MRC5: 1.114507057  JEG3: 2.126402269  U87: 0.804257608  G402: 2.338078135  HCT116: 1.391139917  CRL1690: 0.75310285  AGS: 1.462270254  Panc1: 1.345777182  HMCB: 1.351534041  MG63: 1.847282957  Snu-182: 1.234262395.  Number of positive cell lines: 1.  Mean: 1.886559579.  Mean(log): 1.44115797.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>8224</geneId>
<geneName>SYN3</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2086</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>tttgtgcatgaagctttttctgtaacttagaatctttctttgcgatataattccagaaaatggaaattgtaggttaaaaagctatcctcttaatacatgttgccaaattcctttccagaaggatgtcctaatttacattaccacctgcagtgGGGCAGGAAAGCGCTGTATCTGTTTGCTCTTAAGGGGGTGGAGGTCGTTTCCACTTATGTATTTGTTGGCTTATTTCCAGCAGGTAAATAAAGGCAGCTAAAGCTGACTGCTGGTTGCGCAAAATCCCCCTGGCTCTTCTGGCTAAAGTCCTACCACTCCCTGTACCTGGCAGCAGCCTGTCTTCTGGGCCTCACCTACACACGTCTGGGTAGGAGCCAGTCATCTCCATCCATCCACAGCCATGAATTTCCTCCGGCGACGTCTCTCTGACAGCAGCTTCATGGCCAACCTGCCTAATGGCTATAT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003521</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "tissue inhibitor of metalloproteinase 3 (Sorsby fundus dystrophy, pseudoinflammatory)".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.46460177  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.423731861  HeLa: 1.625590551  HT1080: 0.897152689  MRC5: 1.106604286  JEG3: 0.753808049  U87: 0.729487472  G402: 0.944351109  HCT116: 0.759748383  CRL1690: 1.004715082  AGS: 0.546207398  Panc1: 0.753514492  HMCB: 0.918237929  MG63: 0.856929957  Snu-182: 1.020522743.  Number of positive cell lines: 0.  Mean: 0.877641137.  Mean(log): 0.881471571.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>7078</geneId>
<geneName>TIMP3</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2087</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>gggagtgatacttgtgcttgcttttcctacccacaaagattattgtgagagctataatacggtgagataCAGAATCCTGCTTTTAAAAATACAAAGCAGAATCAAGATGTCAATAATAAGGATAGTAATTGTGTTAGTTATCTGCAATCATCTATTATAGCTAGTCGTCTAGGATCCTGGATCGTTCTCCTGGTTTTACTACAGTTTTGGATCAGCTCACCCCCAAATCCCTTGCTGAAGGGTGGAGCTCTGTCAGCCATGGGCAGGGAACCACTTCCTCTTGCCTTTctactttctgtctttcaaacatgcccagggtctttgcacttgctgttccccctgcctggtacctctctcctgtggcttgccccagagctgatccttgtctttgtccacttctcagcgaggatggcacttcagggagcccttcccttactatcgcagagagagca</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003522</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "tissue inhibitor of metalloproteinase 3 (Sorsby fundus dystrophy, pseudoinflammatory)".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.457142857  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.115456735  HeLa: 0.436494485  HT1080: 0.415446698  MRC5: 1.062436871  JEG3: 0.345152803  U87: 0.552272054  G402: 0.78651923  HCT116: 0.526719546  CRL1690: 0.850257607  AGS: 0.450861552  Panc1: 0.345927389  HMCB: 0.440939307  MG63: 0.453539822  Snu-182: 0.926905798.  Number of positive cell lines: 0.  Mean: 0.487839911.  Mean(log): 0.55063785.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>AK098517</geneId>
<geneName>AK098517</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2088</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>TCTCTTCCCTATCATGGGTCATCTGACCCCTGTCCGTCTCCTTGTCCCTGCTTCATGTTTGGGGGCCTTTCTTTAACTGCCTTCCTGGCTTAGCTCAGATGGCAGATGAGAGTGTAGTCAAGGGCCTGGGCACAGGAGGGAGAGCTGCAGAGTGTCCTGCCTGCCTTGGCTGGAGGGACACCTCTCCTGGGTGTGGAGACAGCTTGGTTCCCTTTCCCTAGCTCCCTGGTGGGTGAATGCCACCTCCTGAGATCCTCACCTCTTGGAATTAAAATTGTTGGTCACTGGGGAAAGCCTGAGTTTGCAACCAGTTGTAGGGTTTCTGTTGTGtttttttttttttttttgaaataaaactataatataaattctcctattaaataaaattattttaaGTTTTAGTGTCAAAAGTGAGATGCTGAGAGTAGGTGATAATGTATATTTTACAGAGTGGGGGTTGGCAGGATGGTGACATTGAACATGATTGCTC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003523</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: "tissue inhibitor of metalloproteinase 3 (Sorsby fundus dystrophy, pseudoinflammatory)".  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.462890625  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.085757787  HeLa: 0.635618745  HT1080: 0.557515568  MRC5: 0.596400237  JEG3: 0.275584266  U87: 0.606023104  G402: 0.259266273  HCT116: 0.425923083  CRL1690: 0.834692332  AGS: 0.34104929  Panc1: 0.229655569  HMCB: 0.415657163  MG63: 0.324503457  Snu-182: 0.955849999.  Number of positive cell lines: 0.  Mean: 0.401423949.  Mean(log): 0.467392634.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>X77690</geneId>
<geneName>X77690</geneName>
<geneSource>USER DEFINED</geneSource>
<geneVersion></geneVersion>
<id>2089</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>ACCCTACAACTGGTTGCAAACTCAGGCTTTCCCCAGTGACCAACAATTTTAATTCCAAGAGGTGAGGATCTCAGGAGGTGGCATTCACCCACCAGGGAGCTAGGGAAAGGGAACCAAGCTGTCTCCACACCCAGGAGAGGTGTCCCTCCAGCCAAGGCAGGCAGGACACTCTGCAGCTCTCCCTCCTGTGCCCAGGCCCTTGACTACACTCTCATCTGCCATCTGAGCTAAGCCAGGAAGGCAGTTAAAGAAAGGCCCCCAAACATGAAGCAGGGACAAGGAGACGGACAGGGGTCAGATGACCCATGATAGGGAAGAGAGGGTGCTGACGGTGTTCAGAATTTCAAATTTTAATTAAAATGAAAAAAAAATGTCAACTTGGAATGTCATGATTTTCTTCAAACAAGCAACGACAACAAAATAGAAGAGATTAAACTATTGGCATATTTAACAGCATTGAACAGAATTCTGTGTCCTGTAAAAAAATTAGCTTATGTCCCCATGTGGGTATA</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003524</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0542 gene product.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.478346457  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 3.278285851  HeLa: 1.897467641  HT1080: 2.158191749  MRC5: 1.197457856  JEG3: 2.799142411  U87: 1.82329496  G402: 2.427503713  HCT116: 2.742467433  CRL1690: 1.087531144  AGS: 2.344677805  Panc1: 2.04971202  HMCB: 1.923154837  MG63: 3.105266116  Snu-182: 1.106554944.  Number of positive cell lines: 5.  Mean: 3.903685059.  Mean(log): 2.138622034.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>9814</geneId>
<geneName>SFI1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2090</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>aggctggtctcaaactcctaacctcaggtgatctgccctcctcggcctcccaaagtgctgggattacaggcgagagccactgcaccAGCCATCTGCTTTCTGCTTGTTGATTTTATTCTTCTTTTTTTTAATCCAGGAAAAAATTACTTTTGAAAGCAGAATGTCCCTCTTAAAGACCCTTTTACCCCACGGTCCCATAGCTTATCATCCTGCTAGGGGATTGCCACTTCCTTGTTTCTAATTTCAGCCTTTCCAGCGTGTGTGCCTTTCTCTTTTCCCTCTCCACCTGTACTTCACCCTGTTTTCCTGCCTCTCCTTTGACTGTTGCCTCTTCTCTGGTTTTCAGGCTTGGTCACAGTGGCGGGAACAGCTCCTGTATGTCCAGAAGGAGAAACAAAAGGTTGTCTCTGCAGTGAAACATCATCAGCACTGGCAAAAACGGAGATTTCTAAAGGCCTGGCTTGAATACCTGCAAGTCCGCAGAGTGAAGAGACAGCAGAATGGTGAG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003525</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0542 gene product.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.476953908  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.600803887  HeLa: 0.770610383  HT1080: 0.984816869  MRC5: 1.066006694  JEG3: 0.736039133  U87: 0.993895227  G402: 0.830062856  HCT116: 0.926685703  CRL1690: 0.205734825  AGS: 0.804836295  Panc1: 1.085153082  HMCB: 1.154037272  MG63: 0.585314417  Snu-182: 1.092694065.  Number of positive cell lines: 0.  Mean: 0.822237733.  Mean(log): 0.845477908.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>9814</geneId>
<geneName>SFI1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2091</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GAGGAGAACAGGCAGCATAGAAAGTGTTAACTCAGTTTTATGAGCTGATTTGGCTCAAAATTTTGTGTTCTTTCAGATCCTAGGCTGTTCTTATTTGAACTTACTGCATCTAAAATTCCTGATCTAACCATTTACAGGAGTCCTACGTCCTACTGAGTGTAAAACATGTTTAAACTCACATTAATTGAGCTTTTACCGCAAATCAAGCACTTACCTCATCAAATCATCACAGAACCCCTAAGAAGCACGTATTTATAGATGAGGCCAGAGAGGTTAATTTACACTCACACAGATGATGTATAAAATGGAGGCAAAGCAGGAAGCCACCCCCAACTCAGACCCCAGCCCACGGTAGCTGCTTTCTCCTCTGTCTGCAGTGCCTGGCCCTGCGGGGAGCGGAGCGGCAGAAGCTGATGCGAGCAGACCTGCACCACCAGCACAGCGTGCTGCACAGGGCGCTGCAGGCATGGGTGGTAGGAACTGCTGCTTCCCTCCTGAT</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003526</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0542 gene product.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.595833333  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 0.526084182  HeLa: 1.692022303  HT1080: Bad Txfn  MRC5: 0.711656948  JEG3: 0.377364754  U87: 1.132880516  G402: Bad Txfn  HCT116: 1.05496243  CRL1690: Bad Txfn  AGS: 0.668657255  Panc1: 0.9460813  HMCB: 0.607912927  MG63: Bad Txfn  Snu-182: 1.146342372.  Number of positive cell lines: 0.  Mean: 0.913218292.  Mean(log): 0.886396499.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>9814</geneId>
<geneName>SFI1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2092</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>AGGAAAGTGACGTTTGAGGGTCCCCTTCTCAACCGCATTGCTGCTGGGGCTGGGGATGGCACCCTTGAGACCAAGAGGCCACAGGCTTCTCGGCCTCTGGGAGCTCTGGGCCGCCTGGCTGCTGAGGAGCCCCACGCCCTGGAGCTGTGAGTAGCCTGTGCTCACCTTGTCCTCGCTTCCACCCTGGGCAAAAGGTTGGATGGCATAGCAGGGAGGAAAACAGCCCTGACGGGATGGGACGGGCTGGTCACGGCCTTGTCACAGCTGAGCTGCTGGGAACCCCCTCTTCTCCAGCCAGATCCCATCCCTCCCACGGCAAGAGGGAGAGAATGGAGTGGGATTTCCAAACCCTCTCTCCTTTGCCTGCCAAAGCTCAGGAAATAGGTGTCCCCTCCTCTGCAACACCTTCCTACCCTCTCTCCCGTCCTGCTGACACGATCTTTTCCGGAGTCATACACGTAGTTGACAAAGGGAACAAGC</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003527</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: KIAA0542 gene product.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.504621072  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 6.50893058  HeLa: 5.142151259  HT1080: 6.902732004  MRC5: 5.932806231  JEG3: 5.495787436  U87: 5.953809603  G402: 5.075852381  HCT116: 4.984777935  CRL1690: 4.120262287  AGS: 7.382522688  Panc1: 4.662636992  HMCB: 6.95417112  MG63: 5.914148147  Snu-182: 3.860670352.  Number of positive cell lines: 14.  Mean: 62.43103819.  Mean(log): 5.63508993.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>9814</geneId>
<geneName>SFI1</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2093</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>GCTTTTAGTCTCTGCACCAGGAATCTCACGTGCTTTCAAATGTTTTACAAAGCACGTAAAAAAGTATTTGAAAAGTCCCACTTACCCCTCCCACTCCTATTTTTAAGATTATTAGGATCGGCCCAAATTTAAAAATTTAACAAAAAGAGTGCTTATTAATTACATTTTAAAATGAAGGGTTACAAAAAGAGATGAGCCTGGCATTTCTAATTCGGGGGCCTTGGGACCTCTCCCCTCCAAGTGCAAGTTGTAGCAACCTGCCGGGTCCACGCATGGGCGGGTCATACTCCACGGGTTCCGGTTTCCACTCCCTGTGAACCAAAAGCCAGAGAGGCCCACGCACGAGTCCGGAAGTGAGGGAGGGAGGACTTTCGTACGCAGCCGCCTCCCAGCTGGAACCTCATCTTTAGTGCTCGGCCGCGGGCGGCGTAACTCGGGGTTCCGCCTCGGAATACCTCCCACTTCTCTTGTCTAAGAGGAGCAGTAGCAAGCTGAGCTCAGAGCGAAGCTGGCGAGCCAAGGAGATAAAGAACCCTCGGTG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003528</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: phosphatidylserine decarboxylase.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the primary publication.  Information on each cell type's results and the number of positive cell lines is available in the evidence comments.  GC Content: 0.698818898  Promoter is soft-masked.</comment>
<date>1-Nov-2005</date>
<userName>smontgom</userName>
</comment>
</commentSet>
<dataset>OREGDS00001</dataset>
<date>1-Nov-2005</date>
<deprecatedByDate></deprecatedByDate>
<deprecatedByStableId></deprecatedByStableId>
<deprecatedByUser></deprecatedByUser>
<evidenceSet>
<evidence>
<cellType></cellType>
<comment>Cell lines tested and results, HepG2: 6.760279418  HeLa: 4.732936983  HT1080: 5.176227049  MRC5: 5.016988583  JEG3: 5.955389142  U87: 3.517595899  G402: 4.27937282  HCT116: 5.22709305  CRL1690: 2.491549769  AGS: 6.118269419  Panc1: 3.878810075  HMCB: 4.98550229  MG63: 5.111421951  Snu-182: 1.753312968.  Number of positive cell lines: 14.  Mean: 34.23814782.  Mean(log): 4.643196387.</comment>
<date>1-Nov-2005</date>
<evidenceClassStableId>OREGEC00001</evidenceClassStableId>
<evidenceSubtypeStableId>OREGES00004</evidenceSubtypeStableId>
<evidenceTypeStableId>OREGET00002</evidenceTypeStableId>
<userName>smontgom</userName>
</evidence>
</evidenceSet>
<geneId>23761</geneId>
<geneName>PISD</geneName>
<geneSource>NCBI</geneSource>
<geneVersion></geneVersion>
<id>2094</id>
<lociName></lociName>
<metaDataSet>
</metaDataSet>
<outcome>POSITIVE OUTCOME</outcome>
<reference>12566409</reference>
<scoreSet>
</scoreSet>
<searchSpace>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</searchSpace>
<sequence>
<end>0</end>
<internalSequenceType>sequence</internalSequenceType>
<sequence>CTGAGTCTGCCTAGTGTTGGGTCGCGGGTGGTGGAGGGGAGGCAGCTGCTTTGGGAGGCCAGCCACGGGCTGCAGACAGGCGGCTCACAGACCAGCGGACAGACTGAGGACAGACAGGAGGCATCCCTTGGGAGCAGCCGGGCCCACCTTGCTGGTTGAGTGGGGTCCTCCCGTGACAGTGACCAAGCAGAGCTGGTGTCTGCTGCCCTTCCCCTTCTCCCTGGCCTTGGCCCTTCCTCTTAAAGGGGCCCTCGGGTTGGGCGGACGGCCCAGCAGGACTGGGGCTCAGAGGGGGCGGCAGCTTTAAGGGTGGCTGGGGTCGGCCTCCTGCCCCCGCCCCTGGTAGTCTGAGTGGCTGGAGCCCGAGCCCCGCCCACTCGCCCCAAGGCTTCCCGGCTCCGGGAGCGCCCCTAGGGAGTCGGAGCCCGGAAGCTGGAGCCACCTGCGGGTGAGTGAGCGGAGCCGGCGCCCCGGCCCTGCCGGGAGCCCCAGGTGACTTCTCAGGGAG</sequence>
<start>0</start>
<verified>false</verified>
</sequence>
<sequenceWithFlank>
<end>0</end>
<internalSequenceType>sequence_with_flank</internalSequenceType>
<sequence>EMPTY</sequence>
<start>0</start>
<verified>false</verified>
</sequenceWithFlank>
<speciesName>Homo sapiens</speciesName>
<stableId>OREG0003529</stableId>
<tfId></tfId>
<tfName></tfName>
<tfSource></tfSource>
<tfVersion></tfVersion>
<type>REGULATORY REGION</type>
<variationSet>
</variationSet>
</record>
<record>
<commentSet>
<comment>
<comment>Promoter description: phosphatidylserine decarboxylase.  This promoter was annotated from a supplemental file from Richard Myer's lab at Stanford.  It has been tested in an increased number of cell types compared to the pr