Tag | Content |
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EnhancerAtlas ID | HS158-10096 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr11:35394470-35395450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr11:35395306-35395321 | GGTCAATGATTAACA | - | 6.06 | HNF1A | MA0046.2 | chr11:35395306-35395321 | GGTCAATGATTAACA | + | 6.72 | HNF1B | MA0153.2 | chr11:35395307-35395320 | GTCAATGATTAAC | + | 6.54 | HNF1B | MA0153.2 | chr11:35395307-35395320 | GTCAATGATTAAC | - | 6.74 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I035373 | chr11 | 35394986 | 35395390 | GH11I035374 | chr11 | 35395403 | 35395808 |
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Enhancer Sequence | AAACTGAGGC ACAGAGGATT TGGGTAACTT GCTCGAACTT GTTTAGCACA TGGTAGTTTG 60 GGATGCAAGC CCAGGCAGCC TGGCTGGGGC ATCTGGCTTC TGCCCACTGC TCACAGCATG 120 ATCAGAGATT CAGGCCTATG TACAACCCAG GGATCCACAT TTCAGAAGCA CGACACACCA 180 GAGCAGGGCA TGAGCCATGT GTGGGGCACT GGGGCACCTT CTCTCAGAGA TGGTGACTTG 240 ATAAAGCCTG GAGGAGCAGG GCCCAGTCAC AGGAAGAGGC AAGGGCGTGT GAGATGGTGG 300 CCACCCCTGC TCCTGCTCAC TGTCCCTTCT GCAGGAGCAG CTGCCCTTTC AGCTCCTTTC 360 TCCATTCAAC ACCTTCTTTC AGACCTCAAG ACCCATGACC AAGTGCTGCT GTTTCCATAG 420 CCAGGTTGGG CCCCCTCATG AATGGGACAA ACCCGGTAGG GATGCCAGTC ATGATCTTCT 480 GCCCCTAGAC TGTGCCAAAC AACAGGTCCC AGGAACCAAG CAAAGGGCTG GGGAGCAGCT 540 GGTCTAGGGA GGGGCTGAGG TCAGGCTGTG GGTGAGAGCA GAAGGTAGAA ACAAGGGTGA 600 GAGAAGCAGA AACAAAGGTT GAGGTACAAG GTGAAACTAA GTGGGAACGC AGGAAAGACC 660 CCAGAAAATG AGTAGATGTG AAACAGGGAG AGGGCTGCAG GCTGTGCTGC AACAAGGTGA 720 GGGGCTGTGG GTGCCCCATC TGCTGGGCAG GAAGTGGTAG GGCTAATGCA GCATGGGCAA 780 GGGGCATACT TGTCTGAGAA CTGGGCAAGG AGCCATTGCC ATGATACAGA GCACTGGGTC 840 AATGATTAAC ACAGCATCCC AGAGTCATAT ACACCAGGAG GCAGAGGAAA CAGAAATCAG 900 ATCATGGGAT TAATATAGCT CAAGTTCAAA GTATTAACTC TGAGCCAGGC ACTTTGCTAA 960 GTACTCCATG CAGATTACCT 980
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