Tag | Content |
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EnhancerAtlas ID | HS076-05461 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:214506160-214507540 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:214506448-214506467 | TAGCCAGCAGGGGGAGCCC | + | 6.93 | RREB1 | MA0073.1 | chr1:214507112-214507132 | TGGGTGGGGGTTGGGTGGGT | - | 6.06 | RREB1 | MA0073.1 | chr1:214507113-214507133 | GGGTGGGGGTTGGGTGGGTG | - | 7.35 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_40820 | chr1:214505971-214507114 | Left_Ventricle |
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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 |
GH01I214332 | chr1 | 214506122 | 214507790 |
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Enhancer Sequence | TAGACACTTC AGGGCTGAGG TGGCCTAGAT GGGATCACTG GAGCTCTTTT TAAAGGCACT 60 GATATTATGC ATTTACAGGG TACGTCCAAC ACCAAGTGGG CCAAGTGAAT CAGGGTCGCT 120 GGGCATTAGA CCCAGAAATC TGTGTTCTGG AAGCATCCCA GGTGTTTCTC AGGAGTTTGA 180 GAAGCCCTCA GTCTCCTTCC ACTTCCGAGA TTAGGGTCTG TGAAGGTTGT GTCTGGTCTG 240 AATGTCCACT GCCCACTCCA CCCTCTACTT ACCCCACTGT GCCCTGATTA GCCAGCAGGG 300 GGAGCCCAAA GGAAGCCAGC TCTTAAAATC TGCTCTTGGA AACAGAATTT GTTAAATTGG 360 GGATAAACTC AAACCTTCCT TTTCTCCTAG AGTGTGTGAG GAAGTGCACT GGCCTCATGC 420 GCAGTTCTCT GTGTGAGATC TGTAGGGAGA GAGGAGCAGA CAGACAGCAT CCCAGCCCTG 480 TGGTTCTCCC AGCAGGGCCT TGCTCTGCTA GACCCATCTT TATCTGCGTG AGCCCCTCCC 540 GGAAGCCCAG CTCTGGTCTT CTGTGGGGCC GTGGGTCCCA GGGCTGCCTC CTACCCAGGA 600 ATACAGCTAG AACATGTCTT TTTGGACTGA CTTTCAGGAG ACACAGGGTG GAACAGCCTA 660 GCCTTTAAAT AAACACCTCT TACACACATG TAAACACACA CACTGGCTCA CCCACCAGCT 720 GCCTCTGGGC CCTGTTCTTA GGGAAATGGC TGTTTCCCAG GCAGACCCCA TCAGTCAGTC 780 TTCAGGTACA GCCGGAGAGA ACACTTGCTG TATCTAAAGC CCCTGCTGGA CAATGGGGAA 840 AGAACATCCA GAAGACACAG GAAGTGTTCT GACTTCAGAG CACTTAACTG TTTTGCTAAA 900 CCAACCCATA TCATAGTGTG ACAGAAAGCT GGGGTCTTAA GACACATTGG GGTGGGTGGG 960 GGTTGGGTGG GTGGCTGTAT GTCTGAGTAC CTAAGGTGAT AGGCCTAATT GCTGCCTTCA 1020 TAAATGGGAC ATTTACTTCA CAAGCTGTTT TCCCAGGGTC TTCCTCTGGG TATGTCTGAA 1080 ATATAAAAAT CTGGACTGGG ATTGAAGATT GTGTTTACAA ATGCTTTTGA ATAGGATTTC 1140 TCCTGCAGTT GTTACGTAGC TTTTCAGAAA CACACAAACT ACAAATAATG AACAACATCT 1200 GCAATGATTC GGCAGGGTGG CAGCATCCAC GCTCTCCACC CAAACCCTGG TGGGATTTGG 1260 AGAGGCCGCT GGTGGGCAGA GGTTGGCCCT AAGCATGGCA GCCTCCGGCT TACTGCACCC 1320 AGCCTGTGGG GCGGCTCAGT AGCCGCTGAC ATGGTGGCCT GTTGTCTCTT CTCTTGTTCT 1380
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