Tag | Content |
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EnhancerAtlas ID | HS147-02354 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:94568770-94570290 |
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 | GATTGGAAAC ACTTGTAACT CAACTCTCAG AGGAAGGTTC TGTTCTTGGG GTCTCTGGGA 60 GCCCCTAGAG GTGAGGCTCT TGCCAGTGGG CTGCCCCCAA CACATTGACT GCTGAAGCAG 120 CTGGGCCCAA TTTAGTAAGA AGGTGGAAAA AGTTAGCCAG GGCTGGATGG GGGTGTCAGA 180 TGCTTTGTGG GGTTGGTCTA GGACAGTGCT TCTCATTGAG GTGGGGCTGG GGAACTGAAA 240 CAGGGGAATT TCATCCTCCT GGAAATATTT GGCAAGATCT AAAGACATTT CTGGGTGTCA 300 CAACTGGGGA GGTGCTGGTG GGTAGAGGCC AGAGATGCTG CTAAACATCC TGCAAGGCCC 360 AAGACACTCC TCCCTCCCCC ACACAAAGGA TTATCTAGCC CCAAGTGTCA GTGATGCTGA 420 GGCTGAGAAA CTCTGGTCTA GGATTGGAGG AGACACGTGC TCTTCCCACA CCGCAGCTGT 480 CACAGGGTAG AGGACCCCTC TGGGTGTTTC TATCATCTCA GCTTGGGCTG AGATGCTCAG 540 GGCACTGACA TGGACTAAGA GAAATGAGTT GGGGCCATTA AGGGCAGGAA AAGCTCCAGG 600 TAGAAAGAGG AGAGCCAGGC ACATGCCGGG GCTTGCCTGA TGAGCCCTAG TCAAGCTCCC 660 TCCAGCTCCT CTCAACACCT GTGGGAAGCA GGGTTTCTTT ATAAGGAGGC ATAAAGAACA 720 CCTAACAGTT AAGGTGACCT TGGGGCAAGT GATTGAGCCT GTCCCCGTGT CTGCATTTTC 780 CACATCTACC TCATAGGATT GTTGATGCGG GGTAAGGAAT GTGAAGTGCT TAGCTCCCAG 840 GCCTCAAAAC AGCACTCAAT AAATGCTTAT TATGATCGAA TTAATATAAT TCTTACCCCT 900 CCTGGGAGAT TCACACAAGC ACCCTCCTCC TCGGCTGGCT TCCAGGGCCA ATGCTTGGCC 960 TCAACCCTGC TAGTGCTATA GTTCATGAGG CTCTGGCCAG AGAAGAGCCT TATGGGCCTG 1020 GATGTCTACG AAGGGACTTC AACACAAAGG GAAAGCACTG GGGTGCGTGA AAATGCCAAT 1080 CTCTTCACCC CGAGTGCTTC AGGGGCATGG GTGACTGTTT ATCTCCCAGT TCTTCTCTAA 1140 CTAGCTTTAA CCATCACATG TCCCCATTCT TTCCTGGTCC CAATTCCACG GCATCCCATC 1200 CTCTTCCTCT CCAAATTCTC CCCTCCCCCA GTGGCCAAGA GGCCTGCCCC TGTGTGCTGG 1260 ACAGCCACCC TTCTCATCCC CAGGTTGTGC CTTTCCCTGA ACAGCACCAT ATCCGGATTT 1320 ATGTTGCAGC TAGTTTCCTC TGGAAGGGTC TTGCGCCAAC CCCACAGGCC TGTCCATGCA 1380 GCTGGGGCAG GGGAAGCCGG TCTTGAAGTT CGACCACACA GTGGCACAGT GGCTTCTCTC 1440 ACAGTAATGG GTTCCCTGAG AGTGGTGCCC ACTGTCACTC CCCTTTGCAT AGGAAAGATC 1500 CAAGGACTTT GGGGAAAGCT 1520
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