Tag | Content |
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EnhancerAtlas ID | HS129-10077 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr13:20993460-20994940 |
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 | TTGCTCTTGT TGTCCAGGCT GGAGTGCAAT GGCAGGATCT CGGCTCACTG CAACCTCTGC 60 CTCCCAGGTT CAAGCGATTC TCCTGCTTCG GCCTCCAAAT AGCTGGGATT ACAGGCATGC 120 GTCACCACGC CCAGCTAATT TTGTATTTTT AGTAGAGACA CAGTTTCTCC ATGTTGGTCA 180 GGCTGGTCTC AAACTCCTGA CCTCAAGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG 240 GATTACAGGT GTGAGCCACC ACATCTGGAT AATTTTGTAT TTTTAGTAGC GATGGGGTTT 300 CTCCATGTTG GTCAGACTGG TCTCAAACTC CTGACCTCAA GTGATCCACC CAGAGTGCTG 360 AGATTACAGG TGTGAGCCAC CACATCCGGC CTAGATTAAG TTTATATTGA GAACTACCAC 420 AATGATTCAT GAGTCTCTCA TGAGAAACTA GTTGGAATTA TGAGTTTGTT CCCTCCACTT 480 ATACATACTG TACCCACATG TTTTCGTTTT CTATACTCTT CACCACATGT TGCTTCCCCC 540 ACATGCAACA GGAAACTGGC TCCACGGCAA GGGTGAAAAA GATCTGACCC AGTGGTTCCC 600 ACCCACGCCA CCTTCCAGGG AGAAGGTGAG GCCAAGATGA GACTTTAATA AGTCGAAAAT 660 AAAAGACTGC TAAGTGCTGC CCCACAATTA CTCACAGGCT TGTGGTCAGG TTTGTGAGCT 720 GCTTGGCCTG TTGCCGGCAC TTACAAGCTT TCTTGGAAGC AAGACACAGA CATTCCTGCG 780 GAATGACTTG AGCAAATTTT GCTAACGCTA CAAGGGTTGA TTGAACACCA CCACATTGAA 840 CTGATGCAAG AGGACACTGA ATCACACCCA TAAAACACCC GTCCTGTCAA GAGTCTTCCA 900 AGAGGACGCG CAGGAGTCAG CGCTCCGGGG AAAGAAGATG AGAAACACCA GGTGGACCAC 960 CCTGGCCAGG CTGCTGGGAA CAAGCCTACG TGCACAGCTG CCGGAGGAGA GGCGGGTCTC 1020 CCCTCTGGGA GGCATCTCAG CTACATCTAT CAAGTTATAA AAATGTTACT CTCCCGCAGG 1080 CTGAGCCCAC TCCCAGAATT ATTCCAGAAA AGACTCCAGA AGAAGAAACC ATATGTGCAT 1140 AGAGGCTCAC TGAGGCCTGA CCTTAAAACA TCCCGCAGTA AGGGAAAGAT TGGATTTAAA 1200 AGAAAAAAAA AAAAGACCAG CTAAATGAAA TATCATAAAG CCATTAAGAA TGAATAAAAA 1260 CTTGAGTAGC ATGTTCATAA TAGAGACTAG ACAGGAACAA AGGAAAATGA AAGCAATTGA 1320 CTTAGGGTAG AGCAAACACA GGTGGAGTTT TTCCCTTTGA CTTTTCTTTA AAATAGAGGT 1380 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTT TTGAGACAGA 1440 GTCTCACTCT GTCGCCCAGG CTGGAGTGCA GTGGCGTGAT 1480
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