Tag | Content |
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EnhancerAtlas ID | HS159-00486 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:207910820-207912400 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr1:207911534-207911549 | AGTTAATCATTAATC | + | 6.17 | HNF1A | MA0046.2 | chr1:207911534-207911549 | AGTTAATCATTAATC | - | 7.85 | HNF1B | MA0153.2 | chr1:207911535-207911548 | GTTAATCATTAAT | - | 6.05 | HNF1B | MA0153.2 | chr1:207911535-207911548 | GTTAATCATTAAT | + | 7.22 | Lhx3 | MA0135.1 | chr1:207912378-207912391 | GAAAAATTAATTT | - | 6.11 | ZNF263 | MA0528.1 | chr1:207911119-207911140 | GAAGGAGAACGAAGATGAGGA | + | 6.58 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I207737 | chr1 | 207910884 | 207912857 |
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Enhancer Sequence | TCTCAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA TTTGTTTCAA 60 CTTTCCCTTT TAAGATTGGA ATTTTGACCA CAGTGTTCCA TGGGAACAAA GTGAATCATC 120 TGTGGCAAAA TATGCTAGTC AAGAAGTGAG TTAGAATCTG TGCCAAGCGT TAAGACCTTG 180 TGCACCCAGG TTCTGGGGCA GAGTGAAGAG GCAGGCTCCA AAGACATAGC TGTGTGTTGG 240 ACATGAGAGT GTTTGGAGGA ATACAGGTAA CAGGTGATGC TGGGAAGTCT TGTGAAATGG 300 AAGGAGAACG AAGATGAGGA ATCTGGTGGC CGTAATAACC GGGGAACAGA TGAGCTGGAG 360 GCCTCATCAG GAGGGGTGTC CCTTGGTGGA AGGACACCAT TCCCGGCCTT AAAAGGAGAG 420 GCTCCAGCAC GGCTGGGGAA GCATGTGGAT ACCTTGTAAT AAATCCACTG TCGTAGCTCA 480 TTCTTGATTG TAATTAAAAG AGGAGGACAT GCTTTCTGAA GCTGACTCCC TCCAAGATGA 540 CCAGTTCCTA TTTCTGTCCC CTGCTACAAC TGTGGTTTAG AGCAAGAGAC TCAAAAAAAT 600 TTCTTCTGTT ATGAGTGACC TGTACGTTTT CTAGAATGGA ATGAGGCTCT TTATTTAGTA 660 GCTCAACTCT GAGAACACTT TTTCTTTGGA CAAAATTAAA AAAGGAAAAG GTCAAGTTAA 720 TCATTAATCT CTCTCTTATC TACTGATGTC TCCATTTACG CCATATTTTC TATGTCCTAC 780 ATAGCAGTCA TCACAGAGGG CAATAAACAC TTCTAATGAC CTTGTAATTT ATATGGAATG 840 CTAGCATCAT GATTATCAGC TTGTAAATTC TGGGTAATTC AATTGTGGAC CATGCTGTTA 900 ATTAAATGAA AACATCCTGT TATTTTAGGG ACCTTCCTTG ACAAAGTACT ATACAGCTGA 960 AGAACATCTC GAATACAATT TTGGTTGGAA AGGAGCCAAT TGATTTCAAC AGAATCAGAT 1020 CTGAGCTTCA TAAAGTCTTT GAAGTGACTT CACAGAGACG CAGACATGTG CACTTGAAGA 1080 TGCTGCCCCT TCCCCGGTAC CTAGCAAAGC TCCTCCCTCT TTGTGTGCGT CACTGTGAAA 1140 CCCCCACCCT TCTGCCTTGT GCTAAACGTA CACAGTATCT AGTCAGGGGA AAAGACTGCA 1200 TTTAGGAGAT AGAAAATAGT TTGGATTACT TAAAGGAATA AGGTGTTGCC TGGAATTTCT 1260 GGTTTGTAAG GTGGTCATTG TTCTTTTTTA AAATATTTGT AATATGGAAT GGGCTCAGTA 1320 AGGAGAGCTT GGAAAATGCA GAAAGTTATG AAAAATAAGT CACTTATAAT TATGCTACCA 1380 CTGATAACCA CTCCTAATAT TTTGATTCAT TTTCTGCCTA TCTTCTTTCA CATATGTGTT 1440 TTTTCACATA CGTACTTTTC CCCCCTTAGT TTCCTTTTAT TTTATAGAGC AGAACCCTAG 1500 TCTTTTAAAG AGTTTAGAGT GAAATATATA CTATATCAGT TTTTACTTTC TCTAGGGAGA 1560 AAAATTAATT TACTAGAAAG 1580
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