Tag | Content |
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EnhancerAtlas ID | HS040-07752 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr12:252600-253470 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr12:253245-253260 | ATGCTGACTCAGCGC | + | 7.27 | MAFF | MA0495.3 | chr12:253245-253260 | ATGCTGACTCAGCGC | - | 7.33 | Nr2f6(var.2) | MA0728.1 | chr12:253281-253296 | GAAGTCCATAGGTCA | + | 6.03 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65535 | chr12:252917-254317 | 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 |
GH12I000144 | chr12 | 252421 | 255424 |
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Enhancer Sequence | GTGATTGCAA AAGTTTCTCC AAGTCCTGAG AATCTACCAC CTTTCCCATC TCTTAGTGCA 60 TTGGTAGCAC TGCCCTAAAC ACTGGGGCAT GATTTGTCAT CCTGCCAGAG CAGCCCACAG 120 GCCCCAGGGC CGTGCTGGGG TGCCAGAGTT CATGCAGGGC AGTGCTGGGG TGCCAGAGTT 180 CATGCAGGGC AGTGCTGGGG TGCCAGCGTT CATGCAGGGC AGTGCTGGGG TGCCAGCGTT 240 CATGCAGGGC AGTGCTGGGG TGCCAGGGTT CATGCAGGGC AGTGCTGGGG TGCCAGGGTT 300 CATGGGGGAA TGAGTTGGCC ATTTGTTATT CATTCAACAA ACATCGAGCA CTTATTTATT 360 GTGTGTTGAG AATGGGGCCA CGCTGGGCAC CCGTGTGTGT GTGTGTGTGT GTGTGTGTGT 420 GTGTGTGTGT GTGAAGAGGC ATGGCTCACA GTCTCAGGGA ACGTACAGAC CCAGGTGTGG 480 ATGGGGAGAG GTGAGAAGCA GGAGCATGGA AAGAGAGTGA GAAGAGCAAG GGGCCTCCAG 540 CCGGAACCCT GGCTTGGGCA AGGTTGAGTG CAGAGCTAAG CCCTGATATG CCCTGGTGAA 600 AGCCGCAATC CCTCATGCTT GATTGTGTAG CCCTGCAGGC CTGGCATGCT GACTCAGCGC 660 CACAGAAAGG AGCCCCTCCC TGAAGTCCAT AGGTCACTGA CTGCCTTGCT TCTCTCCGAG 720 GTGGAGAGGG CCCTGTCCTG CAAAGGGCAG GAGAAGATGG AGAAGCAGAA AGTGGCAGGC 780 ACTAGCAGGG GAGGGGGGCG CTGGAGTCTT TGCATTTCCC TTCCACTCTG ACTGTGTCTT 840 CCTTACTCCC GCCGGAGAAA ACACACACAC 870
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