Tag | Content |
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EnhancerAtlas ID | HS139-26430 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr19:18811080-18812480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr19:18811899-18811913 | GCGGCCTCGGCCTC | + | 6.29 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65614 | chr19:18810064-18812670 | 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 |
GH19I018698 | chr19 | 18809712 | 18812493 |
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Enhancer Sequence | AGGGTGGGCC TTCTCCCACT GCGGGTGCTA ATACCCTGTG CCCATATCCT AGCCACCCTG 60 TCCCTTATCC ACATACCCCA CTCTGGTATT TCAACAGCCC AGAGACCACC ACGGTGCTTG 120 GGGGCTCTCG GCAAGGGGGC GAAGCCTCCC TGAGAACTTC TGCAGGCCGC CCTTCTCTTC 180 CCTTTCCTGC CGGGGCTCTT GCTGCAGAGA AGCTCTCTGC CACACTTTTT TTTTTTTAAA 240 TAAAAAAAAT GAAAATAAAG AAATCATTTA TGTTTCAAAA CTTTGATTAA AATTGAAAAC 300 AGAAACACCA CAGCACTTCC CGTTTCCTCT GCATCTGGCA CCACTCACCT GGGTGCAGAG 360 GGTGGGTGGG TGCATGCCAG CTGGTCATTC GCCCGGAAAT CTCTGGGAGG AAGTATCAGC 420 ACAGCCTAGC AGGGCGCCTG GGACTGGCTC TGTGGGCTGG CCGTCCCTCT GGCTGGGGAC 480 ACGGGGAGGC CGAGCGTGTC CGCAAAGACA CGCGAGCTGT CCACCTTTCT GGGCTGCAGG 540 GGTCTGCAGA ACCTCGGAAC CTCGGAGGGG CTCTCTGTCT GCTTCAGCGT CTCTTTCTCA 600 AGTGACTGAA AGCAGAGGCT CCCTGCTGCG TTACACCATT GAGTCCTTTC GCATCTGTGC 660 GCATCCCGCT TCCATCGCTG CGGGGATCCC TTCGGTCCTC CCAGGCAGGC GAGATTGGTG 720 GCTGTAATTA GGACAGGAGT GGCTCATTAT ATCATCACAG AATAAATGCA CAGACCCTGG 780 GGATGATTTA TGGTCCCAAC AGCCTATCTT TGCGCCCAGG CGGCCTCGGC CTCTGTTCGG 840 CAAGGAGCCC GCTAATCCCT TCACTGCCGG CTCAGCCGGG GCAGAAGGAG GAGCCTGAAG 900 GTCCACCATG GGGTGGAGGC TGCCTGCTCG CGGGCCCGCC CCCAGAGCCC GGGGCTCATC 960 ACGCTGCTCT ATGCGCCTCT GTTGGCTCCT GCCAAACAGT CCCTCCCTTC TGTGCCTCAG 1020 TTTCCTGGCT GTAAAAAGGG GGTGCTCACA GAGCCCCCTT GAGGAGTCGT CACATGGATT 1080 AGATGATGCA TCCACGCAAA GTGTCTGGCC CCGTGCCCGG CCCGTGGTGG GTGCACACCT 1140 TGAAAGATGC CTGCTTGGCC GAGGCCAGCT GTTGAGCTGC TACTTGGGGC AACAGTGAGA 1200 GCAGGATCGC ACCTTGTTCA CCTCTGTGCC TTGGCCCAGA ATATGACAGC TGCCACTGTG 1260 TGGCTTATGG GTCATCTGTT TAGTTTCACC TGAGGGAGTA TTCATTGCTG TTAACTGTTT 1320 CTTATGAGAT AGGATTTTTG TTTTTTGTTT TTTGAGACAG AATCTCACTC TGTCACCCAG 1380 GCTGGAGTGC AATGGCGCCA 1400
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