Tag | Content |
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EnhancerAtlas ID | HS159-00214 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:59679170-59681760 |
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) |
NFE2L1 | MA0089.2 | chr1:59681597-59681612 | CAATGACTCAGCAAT | + | 8.33 | Nfe2l2 | MA0150.2 | chr1:59681595-59681610 | TTCAATGACTCAGCA | + | 6.48 | ZNF263 | MA0528.1 | chr1:59681260-59681281 | GGTGGAGGAAAGGGTGGATGA | + | 6.25 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I059214 | chr1 | 59679747 | 59681155 |
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Enhancer Sequence | GTGTTTTCCA GTGAGCTCTC ATCTGAGAAT AATAGCTTCT ACCAGTTGAT TGCTAACCAT 60 GTGTTTAATC CTAAGTGCAT TATATGTTTA AATTCATTTT GTCATTGGCA CAATACTGTA 120 AAGTATTATG ATTGTCTCCA TTTCACCAGT TGGAAACTAA GGCTTAACAG GTGATGGGAC 180 TTGCTCAAAG TCACCCAGCT ATTAAGAGAT GGAACCAATA TCAAAACCCA GTTATGTATA 240 TCCTCAAGGT CCATGTTCTT AGTCAATATC CTTTACTATT TCCCTTTAAA CTCTACTAAC 300 CAGCATTCCT CTCTTCAGGT AGACATAAAA TCATTTTTCA TAGTGCTGGA AGAGATTTGA 360 AGAACTCACC AAATTCCCAT TTGATTAAAA ATAGAAACAG GGTAGCTGAA GACCTGCGAT 420 GAAGGTTGTC AATTGACAGA AGGTCAAGGA GAAGCACAGC CTTCTACCTC CTGCCACCTC 480 ACAGTGGTCT GCAAAGCTCC TGATATAGGC TGGGTAGTTT CCATTCACTC CTGCAAATTC 540 ACTCTCCAGC CTCAGTCTCT GTGGGGCCCA GTAGCCTACC ACCCATACAC CACATCAACT 600 TTCTGGATTC CAGTCCAATT TGGCATAGGG AAGGCATCCT CAAGAGAGCT GAAGGCAAGA 660 GAGAGAGAGG TTAGGGTCTG TATTCCCTGG TCTCCTTGTG TGGGGCCACA GGTTCTCAGT 720 GGCCATGTTC CTCTAACAAA GGCCTTGACT CCCATCAGGC AGTCCTCTGC CAAATCGCCA 780 GCATAGCTCT TGTGCTCTCT AAGGGCTCTG CTACCCGCCC CTGGTACTTC ACCATCCTGT 840 GTTTATTTCC CTTAATTCCA TCCATACGTT TGTTAATAGT CCCTTCATCA AACTCTTCTC 900 AGTAACCTCA TTTGAGTGGG ATGCTTCCTG TTAGGACACA GGGTAATTCA ATACTAGAGT 960 TTTAGGTGTG GAAGGGATGT CACAGTCTTC TACTCCTGTG GTTTCCAAAC ATTTTATTTT 1020 TACCTGCATA AATCTGGTAA GAACCTCAGT TATGAAACCA ACAAAGTTCT GGAAGTCTGT 1080 GGAACCCTGC CTGCCTAGAA TTTCACCCAA AACACCCCTC TTCCCTGACT CCCCCAAACT 1140 CCTCTGTGAA ACCCAAGGAT TTAGAGCAAA TGCTCCAAAA CCGGCTGACC TAATTCAAAC 1200 CCCTCACTGT ATATGAGGGG AGGAGGCAGT TGGCAAAGTT TCCAAAGTGT CCTTTGTTGG 1260 CCTGAGTGGG TCTGATTTAT GCCCTAGGCC TTCATCAACA GTTTGCCTCA ATATCTTCCA 1320 AAGTGTAAAG TCCCGTAAAT CTTCCCTGAG AGCAACAACT CGACCACCAG TTCATGTTAT 1380 ACAAACACAC AGAAATGTCA TTAAGGCAAC AAACAGCTCT GCTGGCCCCG GCAGAGGCCT 1440 TTTCTGCCAG GCTCAAGTTA CTTAAAATCA ATATTTGAAC AAGGACAAAA CCACATGTTT 1500 TCAAAACCAA ATTAGAAGGG TCTAATACCA GGCCTGGAGA TGTGGTTACA TCACGCGCAT 1560 TCCAGCTGGC CCCTTGGGCC TCTGCCGTTG GGCCTGATCA GCCTGCCCAA GCTCCTACCC 1620 CCTGATACAG TCACTGGACT TACTTGTCCT GAGCATCTGA CCTCACCAGA CAGGTGACAC 1680 TGAGGAAGAG AATAAGCAAG AAATAGGAAC TTTCACAGAG CCAAGCACAG GACCTGAGTT 1740 TACAAACCAA AGCAAGTTAG CTGTGTTCAC TCATTCAATC CTGTCATTTA TTCCAAACCT 1800 GCATGAGACT CTACACTAAG ATCTGGGCAT CCAAAAGTGT ACCAACTCAT GACACTCTGC 1860 TCTCAGGGGA TTTGCAGTAT AGTGTGGAAG GCAGAGAACG CAACGGGACA TTTCAATGCA 1920 GTAAGACAAG TGCCAGTGTT TCAGGTAAGT TCAGGGAGCT GTGTAGGCAC AGGGCAGGGA 1980 CAGGTAACCA GGGCCTGATT GAGGAACTGT CCGAGAATGT TTCCCATAGC AGATATGCCC 2040 AAAGGAACTC TGTCTAACCT ACTATTCTGG CTTTGCTATA TATCAGGCCT GGTGGAGGAA 2100 AGGGTGGATG AGAAGAGAGA AAACCTCTGC CTTCTCCCAG AAGGACCAGG TGTGTGAAAA 2160 AGACTTTTAG CTTCTACCTG GGAAGAGCAC CTGATCTGAT TGGTGAATTG GGATGAGAGC 2220 TGAAGCATGC CCAGCTCAGC ATCTCTGCCC ACTCTCTTTT CAGAGCCAGC CGGTCCAGAG 2280 AACCCCCAAC ACTGTCATCC CCACCACCCA TCGTCTGCTT GAGTAAAGGT GGCCGTGAGT 2340 ACAGGCTCCA TGGCATAAGC CTCTGGCATG GCCCATTCTC AAACAAAATT CTCTCTGAGC 2400 CACATCAGGC TCTTCAGGTT CAGCATTCAA TGACTCAGCA ATGGAGTCAT CATCTTTCTT 2460 AGGACAGTAT TCCGGGCCTT CAGGATCCTG CAGGTGACTG CCACCTGTCT GTGCTCTTCA 2520 CTTGCCCAGT TCCACTGTGT TTCAGGACAC GTCTTCCCTG ATGAGTCAGT GAGCTCTCTT 2580 CTGTCTCCAT 2590
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