Tag | Content |
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EnhancerAtlas ID | HS159-00257 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:84158220-84160500 |
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) |
HSF1 | MA0486.2 | chr1:84160026-84160039 | TTCTCGAATATTC | + | 6.52 | PRDM1 | MA0508.2 | chr1:84158790-84158800 | TCACTTTCAC | + | 6.02 | ZNF263 | MA0528.1 | chr1:84158327-84158348 | GGGGAAGGAAAAGGGGAGGGA | + | 6.26 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I083692 | chr1 | 84157716 | 84160777 |
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Enhancer Sequence | CCTAATGGAT CTGCTGACTT CAGTCCCACA GAGAACGGCC ACTGACTTCA CAGCAGGCAG 60 ACCCATGGAG AGCAAGGGTC AGCCAGCTAC TGAGCATTTA AAACAGTGGG GAAGGAAAAG 120 GGGAGGGAAA TGCCTCTCAG ATAAATCACC GGAGCTGTCT GGGGTGAGCA GTGCCCGTGG 180 TAAGTGAGCT CCTGCAAGTT CCTGTCACAG ACCTGTCCCT TCCACCTCCT ACCCTTAAGG 240 CAGTTCCTGC AGCTCTCACA GCTGTGCCCA CACTTTCACT CCTGCAAAGA ACGTCTCATT 300 GGCTTCAATT GCTTTAGCGG CTCAGCGTGG TCCCTGTCGG GAGCACTTGT CACCTCCTTC 360 CCAAGCAGCC CGCTTGACAC CCAACCTAAT TCCTACTTGG TGAACCAAGC CCCCAAGGTT 420 CCTTTCACCC CCACCCCTGC CCCCCATTTT GTGAAGAGCC AAATTCAGCA GCTCCAATCT 480 CAGCTTTATT TTCATGCAAA GTGAAAGAGC TCAGCCACCC GGCACTGGCT GAAGGGTAGA 540 TAAAAGCCCC AGCTGTGCCT GCTCTGGGAG TCACTTTCAC CTCCAGCAGG AAAGCAAACT 600 GTTTTTGTGC CTGAGGGAAA TTATGGAGCC TCACACTTTC ATCCAGAGAC GGACAAAGGG 660 GAGGTCAGGT GCTGCATCTG CCAGAAATGG GGACGTGTGA AATGTGATTA ACCCAAGGAG 720 AAGCCACACA GAGCCCGGCT GGGGCCTCTC CTGTCCCTGT GTGTTTCCCA GTGTCAGAAG 780 CAGGCAGAAG AGTAAACAAA AGCATTAAAT AAATATTTTT CCGTTTAACC CATGTGTTAA 840 TACAGATTTT TACAACCTCG ACAGCACTGA CTGAATCAAT AGTTGCAAGT ATTAGCCTGA 900 ATAATGAAGG AAGTAGTGTA CATCTGTTGA TTTCTCTGCA TTTGTGAAAA GAAGGGGGGT 960 GGGGGGGTGA GGAGGGGAAG AGATTCCAGA ATGAGCGTGT AATCACATTG TACCCTGCCT 1020 GTCCGCAGCA CAGCTAAGCC TATCGGGCCC ATCAGATGAA CTCGCTAATG CTATTTCTCA 1080 GGCTAAATAC AAACCGCTGG TGCCTGTAGA ATTAAACTCA TCAATAGCTA AGCTCTCCTG 1140 CATTTACAGG AAGACACAAA TAAAATTCCT ACTGATATGC CCATCAGAGT GGGAAGTTAT 1200 CTGTCTCTTT CGAACAGACT TTCTGTAAGA GCTCTGTGTG GTAAATGAAG CTACCAGTAC 1260 ATTTGTCTCT TTGTCAAAAT AAATAATGCC AATTTCATTT TTGAACAGTG TGCTTGGGCT 1320 GTATTCATTA TTGTGTTAGG GTTTTGTTTC CGCCAAAACA GCCCTCCCCA GCCCTGCTGC 1380 TTGGACAACT TGTCTCTGAT TAGGGATGTG TGCTGAAAAC GGAAACTGTT TGAAATTAAC 1440 TAGAGACGTA TTAAATAATC ACAAAAGAAA TTCCGGTAAA AAATAGAGTC AGTTATCAAA 1500 AGATTAACAC GGTTCTTTGT TCCGTTTTTT TTTTTTTTTT TAGACAGGGA GGGGAAGCAA 1560 TTTTCAAGAC AGACACCAAT GCTTTAAAAG GATTTTTCAG AGGTGAATTA CTTAATCCTT 1620 CGTGACTAAG GAAATCTTTG TGTGCACTAC AGAGGATGGG AGCAAAGCAG GAAAAAATGT 1680 ACAATATTGA AAAGTGAAAA TATAATATTT GGCACACTGC AAACATATAA GTTAGAAGGC 1740 CTGTGAGGTG TTTGATACCT GCATCAAATC TTGATTCCTC TCCTATAGGA AGAAGAGGCA 1800 GATATTTTCT CGAATATTCC TAAAGGATTA ACATAATCAG CTATTGAGTG CCACTGCAGC 1860 TACTTCACAA AAATGTAGTT AAGGCGGCAC TTATCTGGCA GTGGGAAACT CAGCTCTGAG 1920 AGAAGGCACT TCATATATTA AGGCTTTAAA TGGTATTTTT TAGGGCACTC TTCACTAAGC 1980 AAGAGCTGCT CTGGAGGTTG AGAGGGGTGT AGCATCCACA GGGCTATTCA GCTCAGTGGA 2040 GCCAGGCATA GGAGAATCTC CCTGTGCCTG CACAGGGCTA CCAGAGAAGG CTGAGAAGCA 2100 GTTCACCTCC AAGGAAGTTC CCATCTGATT CTGTGGAGGG AGGGACTGGT TGAAAGGCAC 2160 AGAACCCAGA CTTCCAGAAA AGCCAGCTCA AAATAGGATT AACCTTTGTT AAAGGAGGGC 2220 TGTGAATTGC TAATACCCTT TAAAACCTGG ATGTGCCCAT GTCTCTGGGG AAACTTCTCC 2280
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