Tag | Content |
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EnhancerAtlas ID | HS146-00789 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:115781290-115782830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:115781949-115781970 | TTCTCCTTCCTTTCCTTCTCT | - | 6.42 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_45728 | chr1:115780312-115784203 | Osteoblasts |
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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: 2 | ID | Chromosome | Start | End |
GH01I115239 | chr1 | 115781333 | 115781470 | GH01I115238 | chr1 | 115781487 | 115782832 |
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Enhancer Sequence | TTGGAAGTCT TTAGAAATTC TTTATCAGCC CCTTGATTTG ACAGACATGA AAGCTTGGGT 60 GCCTGGATTG GCAAGGTCTG CAGAGTAGAA GCAACCTGTC CAAGTTTACA CAGCTGTTAA 120 TGGCTGAGCT GGGATTAGAG CCATGTGAGA TAACGCACCA CCTGGGGTTC TCCCCATTTA 180 TTCCACATCT GTACTGCCTA GCACGTACTT TTAATCTGTA CTTATATATC TTTTATCTCC 240 CCAATAAGAC TGCATTCATT TTACACTGAT TGAACATTTA ATGTGTGCCA GGCACTAGGC 300 TAAGTGCTTT GTGGATATAA AGATGATTAA AATCTGGTTC TTGGATTTAG TGAGCTTCTA 360 ATGCCATAAG GGACTTAAGC AGACTCACAG AATAAGTAGA GTGCTGTGAG ATCATGGTGG 420 AAGGGAGCAT TGTGAGTTCG AGGATCCAAA AAGACTCTAC CAGGAAGCAT GAACTCTCCA 480 AGGGCAGGGA GAATACCTGA CACAACTTGA TATTTTTTCC AGAGTCTTGA ACAGTGTGCT 540 AGAAGCCAGG AGAGTGAGCT GAGACCTCAG CAGAGCTTAC TGTTTTAGAA TTTAGAGAAC 600 TAGCTAAACC TGTTCTTGAT CCCTGCTATG AAGGATGCTA GGGACCAAGA CATTTTGCTT 660 TCTCCTTCCT TTCCTTCTCT CTCTCTCTTT TTTTTTCCTC ATGCCACTCA ATTCTCCTGG 720 GCTCCTCTTC AAAGATTTAA TGAAGATTAA AAATTCACTT TGGAGCCAGG ATATATCATA 780 AGCTGGGAAC AGAGAGGCCA ATGAATCACA CCAGGACCCC TTGCACTGGC TCTGAGGCTG 840 GACTGCACCC AAAGCTGCCT GCAGGAATGA GAGGAAGTTA TGGCATGGAA AGCATTGCAT 900 CTTTGGGCCT TCTCTCTGAG GCAGCATGGA AGCATCCACA GCCCAGTCAG GAAATTCAGA 960 GAAAGAAACG AAACTGATGA CATGGATATT AGGAACACAT TCTTTCCCAC TGAGCCTTGC 1020 TCCCTGGGGT GCAGGCCTAT GGGTTGGTTT GGAACAGAGG CAGCTCTCTG GGTGCCTAGA 1080 CTGGCAAGAA CTGAGATTTG GCCTGAGGCT ACATCAGGTT CCAGATTCCA GTGGTGAGCT 1140 CCAGGATCCT GTGGGGACAG TCTGCTGTGG ACTCTGCCAC CAAGGCCAGG CACTCATTAA 1200 TCTGCACTGG GTATCTGCAA CAGGAGCCTG GTCTGAGGTA GGTAAAGGGG TTGGGAAGGA 1260 CAGAGCCATG AGAGTCATTA GGTTTTAAAA GTCAGCTTTA TTCTTCTCTT ATTAGGTTGA 1320 CCTAAGTGCA CAAAATCAAT TTTCCAAAAC TAAGAAGGAC TTCATGTTAC TGATAGGTTG 1380 GTTGGAATAC AGAGCCTCTA AAGTTCTTTT CATCTCAGAA ATCTGGAATT CCATAAGAAG 1440 GACTTTGAAA GAGCCCATGT ATCTTCTGCT TTTTCTTTGT CATGATGTTA TCATTCTCAT 1500 TTACTAGCTG GGTGACCTTT GGCTCTTACC TTTTCTAGAT 1540
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