Tag | Content |
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EnhancerAtlas ID | HS118-05132 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr13:21120780-21122720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr13:21121888-21121903 | TGTTAATGATTAACT | + | 7.7 | HNF1A | MA0046.2 | chr13:21121888-21121903 | TGTTAATGATTAACT | - | 8.03 | HNF1B | MA0153.2 | chr13:21121889-21121902 | GTTAATGATTAAC | - | 7.52 | HNF1B | MA0153.2 | chr13:21121889-21121902 | GTTAATGATTAAC | + | 7.82 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35607 | chr13:21120981-21122706 | HepG2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 21120800 | 21120919 | chr13 | 21121764 | 21122087 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I020546 | chr13 | 21120461 | 21122494 |
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Enhancer Sequence | GCTCAAATAG CTCTACAGAC CTAGAGCAAT GCCAAATCCT ATGCTCTCTT CACCACAAAT 60 TATCTGAAAC TTCCTCTTCT TTTACATAGC CCAGCCCTGC TTCCTCTCTG AAGCTGTGGC 120 TACTCCACCC ATAATAGAAA TTAACTGCTT AAAGTAGTAA AAAGAACTCT GTACAGCATG 180 TGTAATTGAA CTAGATTCAC TGAACTAGAA CAACTCATGG GATGTAATTC AAGCCCAACT 240 TTATTTTTGT CTCCCTTTCC CCTTTTAAAA CTTAGGTGGG GCCCTGATTT TTCTGATCAC 300 TTTGGGGAAA TAAAAGCCTA AGGGTAATTT AAGTTGCAAA TACAGTCTTA ATTAGGTCAT 360 TAAATCTCCC CTCTTGCCAG CTGGGACCAG TCGCAGAGGA ACACTTTGAA GGTGAAATCC 420 CAACTCTCCA TCCTTTACCC CAATACTAGT AAGAGATCAA AAAGTTCCAA AACATTCTGG 480 ACCACCTACT TTGAAAAAAT GCACATTGGT CTGGCAATTC ATTTTTACAT CTGTGATCTG 540 TTATCTTAGG GCATCAGCCG TAATCCCCAA CTTAACGTGT TGCTACATAG GTAACAGTAT 600 ACAAGTCAAT ATCAGAAAGG CAAAACTGTG CGGTGGTTAA AAGTGTGAGC TCTGGAGTCA 660 GATTGCCAGG GTCTGAATCT CAAATTCATA TTTTGCTACT TGCATGATTT TATTTTTATT 720 TTTATTTATT TTTTCTGGAG ATGGAGTCTT GCTCTGTCGC CCAGGCTGGA GTGCAATGGC 780 TTGATCTCCT CACTGCAACC TCCACCTCCC GGGTTCAAGC AATTCTCCTG CCTCAGCCTC 840 CCAAGTAGCT GGGACTACAG GCGCACACTG CTATGCCTGG CTAATGTTTT GTATTTTAGT 900 AGAGACAGGG TTTCAATATG TTGCCCAGAC TAGTCTTGAA CTCCTGAGCT CAGGCAATCC 960 GCCCATCTTG GCCTCCCAAA GTGCTAGGAT TACAGATGTG GGCCACCGTG CTTGGCTAGT 1020 TGCATGATTT TAGACAAGTT AGTTCCTCAA AACTCAGCCT TTTCAGCAGT ACAATGGTCA 1080 TAATAGAGGT TCCCTCTTAA AGGGTTATTG TTAATGATTA ACTGATAGAA TCCATTCTAA 1140 AATGTGCTTG GCACATGGCC AGTGTTGGAT CATTCTGTGT CCTCTGTAGT ATCACGCAGC 1200 AGCTCTTCCT TACACATACT CTCACTTGGC CCTCCCTGGC ACCTCCCTGG CATATGTAAA 1260 GCAGATTCCA GCCCCACCAT TCTACAGGTG ACAGCCCCAA GACTTCCAGG CCACTTAGCA 1320 GGTCCATCTC AGACCAGATC TTTCCTTTCT AGTCAAAATG TCTTGAATTA TATATTTATC 1380 CTAAACTTGA ACAGTGTTTT ACAAAAGATG AATTTGAAAA CTCAGGCATA GTCTCCAGGA 1440 ACATGCAAAG GCATTGCAGG GTCATAGCAA ACTAGTTCAT AAAACCAGTG CACACGTCGC 1500 TGCTTATGTC TGTTCCTATC CCCTGTCTAA ACACACTGGT CATAGGTCCT TCTCCTCCTG 1560 TCCACTTCTG ACATCCTTTA AAATATCACA AGTAATAGCT TACATTAATA CTGCACTTTA 1620 CAAATGCTTT CTGATCATCC ATCCCTTGCC TATATTTATT TTGCTTAGAA AGGAAGGTCG 1680 GGCAAGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGCAG GATTGCTTGA 1740 GCCCAGGAGT TCGAGATCAG CCTGGGCAGT ATGTCAAGAT CCTATATCTA TGAAAAAAAA 1800 ATTTTTTTTT TAATTATCCA AACATGGTGC TATGTGCCTG TGGTCACAGC TACTAGGGAG 1860 GCTGAGGTAG GAGGATTGCT TGAGCCCAGC AGGTCAAGAT GGCAGTGAGG TTTGATTGTG 1920 CCACTTCACT CTAGCCTGAG 1940
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