Tag | Content |
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EnhancerAtlas ID | HS154-11161 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr19:18811000-18812410 |
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 | TCCGCTGGTC CCAGGAGTTT CACTCCGTGG GGTGGGGTTG AAGGGTGCGG TGAGGCCCAG 60 AGGGGCTGAG TCTGCTTGGA AGGGTGGGCC TTCTCCCACT GCGGGTGCTA ATACCCTGTG 120 CCCATATCCT AGCCACCCTG TCCCTTATCC ACATACCCCA CTCTGGTATT TCAACAGCCC 180 AGAGACCACC ACGGTGCTTG GGGGCTCTCG GCAAGGGGGC GAAGCCTCCC TGAGAACTTC 240 TGCAGGCCGC CCTTCTCTTC CCTTTCCTGC CGGGGCTCTT GCTGCAGAGA AGCTCTCTGC 300 CACACTTTTT TTTTTTTAAA TAAAAAAAAT GAAAATAAAG AAATCATTTA TGTTTCAAAA 360 CTTTGATTAA AATTGAAAAC AGAAACACCA CAGCACTTCC CGTTTCCTCT GCATCTGGCA 420 CCACTCACCT GGGTGCAGAG GGTGGGTGGG TGCATGCCAG CTGGTCATTC GCCCGGAAAT 480 CTCTGGGAGG AAGTATCAGC ACAGCCTAGC AGGGCGCCTG GGACTGGCTC TGTGGGCTGG 540 CCGTCCCTCT GGCTGGGGAC ACGGGGAGGC CGAGCGTGTC CGCAAAGACA CGCGAGCTGT 600 CCACCTTTCT GGGCTGCAGG GGTCTGCAGA ACCTCGGAAC CTCGGAGGGG CTCTCTGTCT 660 GCTTCAGCGT CTCTTTCTCA AGTGACTGAA AGCAGAGGCT CCCTGCTGCG TTACACCATT 720 GAGTCCTTTC GCATCTGTGC GCATCCCGCT TCCATCGCTG CGGGGATCCC TTCGGTCCTC 780 CCAGGCAGGC GAGATTGGTG GCTGTAATTA GGACAGGAGT GGCTCATTAT ATCATCACAG 840 AATAAATGCA CAGACCCTGG GGATGATTTA TGGTCCCAAC AGCCTATCTT TGCGCCCAGG 900 CGGCCTCGGC CTCTGTTCGG CAAGGAGCCC GCTAATCCCT TCACTGCCGG CTCAGCCGGG 960 GCAGAAGGAG GAGCCTGAAG GTCCACCATG GGGTGGAGGC TGCCTGCTCG CGGGCCCGCC 1020 CCCAGAGCCC GGGGCTCATC ACGCTGCTCT ATGCGCCTCT GTTGGCTCCT GCCAAACAGT 1080 CCCTCCCTTC TGTGCCTCAG TTTCCTGGCT GTAAAAAGGG GGTGCTCACA GAGCCCCCTT 1140 GAGGAGTCGT CACATGGATT AGATGATGCA TCCACGCAAA GTGTCTGGCC CCGTGCCCGG 1200 CCCGTGGTGG GTGCACACCT TGAAAGATGC CTGCTTGGCC GAGGCCAGCT GTTGAGCTGC 1260 TACTTGGGGC AACAGTGAGA GCAGGATCGC ACCTTGTTCA CCTCTGTGCC TTGGCCCAGA 1320 ATATGACAGC TGCCACTGTG TGGCTTATGG GTCATCTGTT TAGTTTCACC TGAGGGAGTA 1380 TTCATTGCTG TTAACTGTTT CTTATGAGAT 1410
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