Tag | Content |
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EnhancerAtlas ID | HS176-10808 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:20993550-20994910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr13:20994757-20994778 | CAAAGGAAAATGAAAGCAATT | - | 6.91 | IRF2 | MA0051.1 | chr13:20994761-20994779 | GGAAAATGAAAGCAATTG | + | 6.8 | ZBTB18 | MA0698.1 | chr13:20993718-20993731 | CCACATCTGGATA | - | 6.5 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26953 | chr13:20992871-20994791 | Esophagus |
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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 |
GH13I020418 | chr13 | 20993028 | 20994960 |
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Enhancer Sequence | GCCTCCAAAT AGCTGGGATT ACAGGCATGC GTCACCACGC CCAGCTAATT TTGTATTTTT 60 AGTAGAGACA CAGTTTCTCC ATGTTGGTCA GGCTGGTCTC AAACTCCTGA CCTCAAGTGA 120 TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCACC ACATCTGGAT 180 AATTTTGTAT TTTTAGTAGC GATGGGGTTT CTCCATGTTG GTCAGACTGG TCTCAAACTC 240 CTGACCTCAA GTGATCCACC CAGAGTGCTG AGATTACAGG TGTGAGCCAC CACATCCGGC 300 CTAGATTAAG TTTATATTGA GAACTACCAC AATGATTCAT GAGTCTCTCA TGAGAAACTA 360 GTTGGAATTA TGAGTTTGTT CCCTCCACTT ATACATACTG TACCCACATG TTTTCGTTTT 420 CTATACTCTT CACCACATGT TGCTTCCCCC ACATGCAACA GGAAACTGGC TCCACGGCAA 480 GGGTGAAAAA GATCTGACCC AGTGGTTCCC ACCCACGCCA CCTTCCAGGG AGAAGGTGAG 540 GCCAAGATGA GACTTTAATA AGTCGAAAAT AAAAGACTGC TAAGTGCTGC CCCACAATTA 600 CTCACAGGCT TGTGGTCAGG TTTGTGAGCT GCTTGGCCTG TTGCCGGCAC TTACAAGCTT 660 TCTTGGAAGC AAGACACAGA CATTCCTGCG GAATGACTTG AGCAAATTTT GCTAACGCTA 720 CAAGGGTTGA TTGAACACCA CCACATTGAA CTGATGCAAG AGGACACTGA ATCACACCCA 780 TAAAACACCC GTCCTGTCAA GAGTCTTCCA AGAGGACGCG CAGGAGTCAG CGCTCCGGGG 840 AAAGAAGATG AGAAACACCA GGTGGACCAC CCTGGCCAGG CTGCTGGGAA CAAGCCTACG 900 TGCACAGCTG CCGGAGGAGA GGCGGGTCTC CCCTCTGGGA GGCATCTCAG CTACATCTAT 960 CAAGTTATAA AAATGTTACT CTCCCGCAGG CTGAGCCCAC TCCCAGAATT ATTCCAGAAA 1020 AGACTCCAGA AGAAGAAACC ATATGTGCAT AGAGGCTCAC TGAGGCCTGA CCTTAAAACA 1080 TCCCGCAGTA AGGGAAAGAT TGGATTTAAA AGAAAAAAAA AAAAGACCAG CTAAATGAAA 1140 TATCATAAAG CCATTAAGAA TGAATAAAAA CTTGAGTAGC ATGTTCATAA TAGAGACTAG 1200 ACAGGAACAA AGGAAAATGA AAGCAATTGA CTTAGGGTAG AGCAAACACA GGTGGAGTTT 1260 TTCCCTTTGA CTTTTCTTTA AAATAGAGGT TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 1320 TGTGTGTGTG TGTGTGTGTT TTGAGACAGA GTCTCACTCT 1360
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