Tag | Content |
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EnhancerAtlas ID | HS095-01524 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:94568790-94570110 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:94569240-94569251 | CCGCAGCTGTC | - | 6.32 | TP53 | MA0106.3 | chr1:94569389-94569407 | CACATGCCGGGGCTTGCC | + | 6.17 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33968 | chr1:94568993-94570002 | HCC1954 |
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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 |
GH01I094099 | chr1 | 94565390 | 94573062 |
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Enhancer Sequence | CAACTCTCAG AGGAAGGTTC TGTTCTTGGG GTCTCTGGGA GCCCCTAGAG GTGAGGCTCT 60 TGCCAGTGGG CTGCCCCCAA CACATTGACT GCTGAAGCAG CTGGGCCCAA TTTAGTAAGA 120 AGGTGGAAAA AGTTAGCCAG GGCTGGATGG GGGTGTCAGA TGCTTTGTGG GGTTGGTCTA 180 GGACAGTGCT TCTCATTGAG GTGGGGCTGG GGAACTGAAA CAGGGGAATT TCATCCTCCT 240 GGAAATATTT GGCAAGATCT AAAGACATTT CTGGGTGTCA CAACTGGGGA GGTGCTGGTG 300 GGTAGAGGCC AGAGATGCTG CTAAACATCC TGCAAGGCCC AAGACACTCC TCCCTCCCCC 360 ACACAAAGGA TTATCTAGCC CCAAGTGTCA GTGATGCTGA GGCTGAGAAA CTCTGGTCTA 420 GGATTGGAGG AGACACGTGC TCTTCCCACA CCGCAGCTGT CACAGGGTAG AGGACCCCTC 480 TGGGTGTTTC TATCATCTCA GCTTGGGCTG AGATGCTCAG GGCACTGACA TGGACTAAGA 540 GAAATGAGTT GGGGCCATTA AGGGCAGGAA AAGCTCCAGG TAGAAAGAGG AGAGCCAGGC 600 ACATGCCGGG GCTTGCCTGA TGAGCCCTAG TCAAGCTCCC TCCAGCTCCT CTCAACACCT 660 GTGGGAAGCA GGGTTTCTTT ATAAGGAGGC ATAAAGAACA CCTAACAGTT AAGGTGACCT 720 TGGGGCAAGT GATTGAGCCT GTCCCCGTGT CTGCATTTTC CACATCTACC TCATAGGATT 780 GTTGATGCGG GGTAAGGAAT GTGAAGTGCT TAGCTCCCAG GCCTCAAAAC AGCACTCAAT 840 AAATGCTTAT TATGATCGAA TTAATATAAT TCTTACCCCT CCTGGGAGAT TCACACAAGC 900 ACCCTCCTCC TCGGCTGGCT TCCAGGGCCA ATGCTTGGCC TCAACCCTGC TAGTGCTATA 960 GTTCATGAGG CTCTGGCCAG AGAAGAGCCT TATGGGCCTG GATGTCTACG AAGGGACTTC 1020 AACACAAAGG GAAAGCACTG GGGTGCGTGA AAATGCCAAT CTCTTCACCC CGAGTGCTTC 1080 AGGGGCATGG GTGACTGTTT ATCTCCCAGT TCTTCTCTAA CTAGCTTTAA CCATCACATG 1140 TCCCCATTCT TTCCTGGTCC CAATTCCACG GCATCCCATC CTCTTCCTCT CCAAATTCTC 1200 CCCTCCCCCA GTGGCCAAGA GGCCTGCCCC TGTGTGCTGG ACAGCCACCC TTCTCATCCC 1260 CAGGTTGTGC CTTTCCCTGA ACAGCACCAT ATCCGGATTT ATGTTGCAGC TAGTTTCCTC 1320
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