Tag | Content |
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EnhancerAtlas ID | HS091-00739 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:21920250-21922700 |
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) |
CTCF | MA0139.1 | chr1:21922203-21922222 | TGGCGCCGCCTTGTGGCCA | - | 6.59 | MAX | MA0058.3 | chr1:21920920-21920930 | ACCACGTGCT | + | 6.02 | Nr5a2 | MA0505.1 | chr1:21921838-21921853 | GAGTTCAAGGCCACA | + | 6.65 | ZNF263 | MA0528.1 | chr1:21921153-21921174 | GGAGGTGGGGCAGGAGGAGAG | + | 6.71 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33659 | chr1:21911996-21920758 | H2171 | SE_65280 | chr1:21921409-21922251 | Pancreatic_islets |
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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: 1 | ID | Chromosome | Start | End |
GH01I021594 | chr1 | 21921410 | 21922251 |
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Enhancer Sequence | GCTGCTGTTT CCACTACCAG AGTAATTTCT AAGCAGAGTC CAGCGCTTCC CGGAGCCTGG 60 TACCCCCCGC CCAAGTTCTA ATTCCAGCCT CGAGTCAGAG TGTCCCGGCT CGCCCTCCCA 120 CCTCACAGCC CAGGGTGAGC ACAGAGCTGG CGCGGGCACA AGAGAAATAG CACCGGACAC 180 TTTGATCCCA GAGGCCCGAT CCGTTGCCAG CCTCCCCTGA CCCCACCTCG GAGCTTGGAG 240 GGATGCGGTA GGGTGAAACC CAGCCCCAAG GCCTTCCTTC CCGCAGACGG CCTGGCACCA 300 GCTGGACAGG GATGGGGCAA AGGCAGGTTC TGCCCACCAA GCTGCCCACC TGCTCTGCCA 360 CAGCAGCCCC TGCTGCTCTG TCTCAGCTGT GGGATAGAGT GGAGTGGGGG TGCATTGCTA 420 AGTACAGGGA GACAAGCCGG AGACCTCCCC CAGCTCTGTT ATGGCAGCAT CGTCACCCCA 480 GGTAAACCTG GCAAGCTGAG GCCCAGGGAA GCACCTGACG CCGTCCATTC CCAAAGCCTC 540 ACATCTAGGC ACCTGTGCTG GGCCCAGTGG CAGGTGGGCG TCCTCCACGC ACTGAGCGGA 600 CCCCACGTGT TCTGAATTAC GGACGTCATT GATCCCTTCC TGCGGTATGC ACACTCTCTT 660 CTTTGAGCCC ACCACGTGCT GGGGCTGCAC CCAGAACTTT ATGAGGTGTC ACCTCATTTA 720 ATCCTCATGC CAGGGTGCCA GCGAGGGCAG GGCTGTTAGC ACCCCCACTG CACAGATGAG 780 GAAACTGAGG CCCAGGGAGC CAAAATCGTG TCTGCATGGT CATAGCGCGA GGAGGCGAAG 840 CAGCTCAGAG CTGATTCTGA AGAAGCTCTT AACCGTGGTG CTGAACTGTG ATGCCGGCCC 900 TGTGGAGGTG GGGCAGGAGG AGAGAGGGCA GAGGACTGCG GCGGAGGGAT AGGGAGCAGG 960 GGTGCGGCTG ATGGGTGGGC AGTTCACAGG GGACTCACTG GGCCCAGAGC AGCCTAGAGC 1020 CAAACCGAGT TGGGTGGGGC TGGGGTTTGG GTGTGAGTCA CCACCCATGG GTGGCCTGAG 1080 GCATCAGAGG GTCACAGAAG GGCCCTGTCG GGAAAAGTGT GGCACTCCCT GGACAAACCC 1140 CTGGGGTTCC TTCAGCATCA TCCTGGGAAG GGGGCAGGGC CAGCAGGGGA TAGGGGGCAC 1200 TGCCAAGCTG TCAGGGAGGC CAAGGCACGG CTCATCCCTT CGGGGCCCAA TTTGGTGCCT 1260 ACTCCCAAAT GTCCCCAAAG CCACCCCGCA GACCTGCTCT CCTCCGTGGT CCTGCCCCAG 1320 AGGGAGAGTC CCCTCATTCA CCCAACACCC AGCCTGTACC CCCGGGAGCC ACCCGATTCC 1380 CCCCTTAGCC CCACAGCCCA TCAGGCGCTT GGTCCCCCTG CTCAGGCCCA CCTGGTGTCC 1440 TTCTCAGCGT CCTCCTGGCC ACCCTCTTAC CCCAGCAACA ACCTCGTTGG TCCCCTCCTC 1500 CCTCCACTGG TGCAGCCTCC ACCAGCAACT ACCGCTCCTG CCTGGGGCTC CCCCTGCCCT 1560 TGGCGCAGAG CCCTGGCCTC TCCGTCGGGA GTTCAAGGCC ACATTGCCTC TGGCCTCATC 1620 CCTGCCCATC TCCCTGTCCC CTCCATTGTC ACCTTCCCAC CATTCAGAGC TGGCTGCCAC 1680 CTTCCTGGTT CCAGGGGTGC TCTGCCTCCC CGCCCTTTAC TCGAGGCCCC CTCCTGCAGC 1740 GTCCCTCCTC CCTAGGCCTT CTCAGGAACG GGGAGCAACT CCAGGAACTT TCCCTGACGC 1800 CTCTCTCCCC AGGCCCTGCT TGTGCACACC TCTCCTGTCC CCGGCTGCCC CTCATCACCC 1860 TTCGTCCTAC TGTCCCAGCT GTGAGATCCT GGTAGAGGGA CTTGGACTCA TCCCCGTCTC 1920 CTGGGTCCCC ATCGGGTCCC GTAAGTGGTC CCTTGGCGCC GCCTTGTGGC CATATCAGGG 1980 GATTCACTGA ATATGAGAAC AGGGAGAAGG AAGTAATTAA TTGAGCACCT AATGTGTGCC 2040 AGACACTGTG CTGTATGTTT GATACGCACC AGCTCATTGA ATCCTCACAA CAAACCCTTG 2100 GGAGAAACAC TACCACTCCT ATTTTACAAA AGGAAACACT GAGGCTCACG GAAGCTAGTA 2160 AGTTTCTCAA CGCCACCCAC CCAGCTAACA AGAGACGGTC CCAGGACTCA AACCTAGGTC 2220 TGCCTGACAG CACAGCCATG TTCTTCCTGC AGTGGGGAAG GGGCCCAGGA TGCAGGGAAG 2280 GACAGCACCC CGGGGAGGAA ACCACGGGCG GTGCTCACAG AGCTGGTGGC TTGGCTTTGG 2340 AGGTGTCCCC AGGCCCAGCA GCTCTGATGG GGACAGGCTT GCTCCCTGCC ACCTTGACAT 2400 CCCTGGACAT CTGTCTGGGG TCAATCTGGC CACGGTTCAC ACAAAGCCAG 2450
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