Tag | Content |
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EnhancerAtlas ID | HS127-32539 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr9:131636340-131637660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr9:131637450-131637461 | AACAGCTGCAG | + | 6.02 | SOX10 | MA0442.2 | chr9:131636927-131636938 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr9:131636928-131636938 | CCTTTGTTTT | + | 6.02 | Tcf12 | MA0521.1 | chr9:131637450-131637461 | AACAGCTGCAG | + | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26602 | chr9:131636414-131636845 | Esophagus | SE_36103 | chr9:131636939-131637746 | HMEC |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 131636805 | 131637114 | chr9 | 131637417 | 131637477 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I128874 | chr9 | 131636511 | 131638732 |
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Enhancer Sequence | CCTGGTCAAC ATGGTGAAAC CCCGTCTCTA TTAAATACAC AAAAATTAGC CAGGCGTGGT 60 GGCGGGCGCC TGTGATCCCA GCTACTCAGG AGGCTGAGAC GGGAGAATCG CTTGAACCCA 120 GGAGGCAGAG GTTGCAGTGA GCCGAGATCA CGCCACTGCG CTCCAGCCTG GGCAACAAAA 180 ATGAAACTTC ATTCCAAAAA AAAAAAAAGA ATATTCTGAA CTGAACAGTG CTGCAGTCTT 240 CCAGTGGTTT AATTTAGGAT ACAGAATGAG CATTTCTTCT ATGTTTGTTG CCAAGGCTGG 300 AGTGCAGTGG TGTGATCTCG GCTCACTGCA GCCTCAACCT ACCGGGCTCA GGAAATCCTC 360 CCACCTCATT CTCCTGAGTT GCTGAGACAA TAAGCACGAA CCACCATGCT CAGCTATTTT 420 TTTTTTTTTG TAAAGATGGG GGTTTTACTA TGTTGCTTAG GCTGATGTTG AACTCCTGGC 480 ATCAAGCAAT CATCCTGCCT TAGCCTCCCA AAGTGCTGGG ATTACAGGTG TAAGCCACTG 540 CACCTGACAT CTTCTATGTC TTGATGAATA CGAGTCATCC TTAGTCATCC TTTGTTTTCA 600 ATGTTGTGAA ATATCTCTGG GAGTTCCTGT TCTGTACATT TTGTGGTGAG ATAATCCTGC 660 CTTTTTTTTT TTTTTTTTTT TGAGACGGAG TCTCGCTCTG TCACTCAGGC TGGAGTGCAG 720 TGGCGTGATC TCGGCTCACT CCAATCTCTG CCTCCCAGGT TCAAACGATT CTCCTGCCTC 780 AGCCTCCTGA GTAGCTGGGA TTACAGGCAC GCACCACCAT GCCCGACTTA TTTTTGTATT 840 TTTAGTAGGG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC TGACCTCAAG 900 TGATCTGCCC ACCTCGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACTGCGCTCA 960 GCCCAGGGAG TTCCTTTAAT GTGAAGTTTT GCTGGTATTA TTTCCTCTGG GTCATTATCT 1020 TTTTCTTTAG AACCACTTTC CTCATTTATG TTGATAAGTT TGCCTTCAAG AAGTTTCTCT 1080 GGATGCAGAT CTCAGGTTTC CCAAACTGTG AACAGCTGCA GAGTTGCCAT CCCCACAGCT 1140 AGCTATTTCT TCCATTATTC CATTTATGTT CAATTTGTTT TTTTTTGTTT TTTTTTTTTT 1200 TTTGGTTTTT GTTTTTGAGA TGGAGTCCTG CTGTGTCGCC CAGGCCGGAG TGCAGCTGTG 1260 TGACCTTGGC TCACTGGCGT GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA 1320
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