Tag | Content |
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EnhancerAtlas ID | HS040-03270 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:212415400-212416640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:212416184-212416199 | GGGGTCAAGGTCAGA | + | 6.15 | RREB1 | MA0073.1 | chr1:212416426-212416446 | CCCCACACCTCCCCCAGACC | + | 6.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_00506 | chr1:212413973-212416930 | Adipose_Nuclei | SE_31662 | chr1:212415272-212416732 | Gastric |
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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 |
GH01I212241 | chr1 | 212414762 | 212416742 |
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Enhancer Sequence | TCCAGTGAAA AAATAATTGC AGTGAATCTC TCCCTGACTT GGCCCCCAAA GAGGCAGACC 60 TAGGTATTTT AGGACCTGAG TCAAGTTTGA AGAACTGTGC TGTCTCTTCC CAACCTTCTC 120 TTCAGAGAAC TAAACCACGG GGGTAACAAT CCTGTAATTT TGGCCGTATT TATAAATCCC 180 TGATCCTTTA TGTAGCGCAT TTTTTCTACT CTGCGCTTAG TCTGAATGTT GCTATTTTCA 240 CAGAGGAAAT CAGAGGAAAG AGACTATAAT TATAGGTCAA ACACCAGCTC CGGAAACAGT 300 GAAGGCAGCA GAGAGCCTAT GACTCCCTGC CCTCTTCCGG GTTACACCCT GGACATCTCC 360 CCGTTCTTTC CTGGAGCCTA GGTCAGCTCT TCGCCTCTTT ATCTTCATAT CTTTGCTGTC 420 TTGTTTTCCA GTCCAGCATA TCATGAGACA AAAAGGGAAA GTTACAACCA AAAGCCAGTG 480 AGTTAAAACT GCACGATACT TGGGCAAGCC TGCCTCTTGG AGATAATTCA AATGGAAAAG 540 AAAAGACAAA AAACCCCACA ACATTTCAGG TCATTGGCCT TTTTAAACAG ACCGCCGGCA 600 ATATTTACTC CTCCTGAAAT AGCACAGTCA CATGAAATAA AACCGTGTTC GGTAAAGCCT 660 GCAAAACAAA AGGACAACTT ACAGGCTGGC ATGCTCACTG AGGGCCTTCT GTTTACCGGC 720 CAGATCAGGG CTCTGCTTCC GGGCTCTCTA GCCACCTTCT GCCCAAACCT GCTGGAGAGC 780 TGTGGGGGTC AAGGTCAGAT TTTCTTGGAG ACCCTCCCCA CTCTTTTCCC CTTAAATGAT 840 TTGGAAAGGC AGGTTGAGAG TTGGGAACAG GGCTGTGAAG AGTATGTGGC TGATGTGGCC 900 TCTACTGTAG AAGCCCAGGT TGTGAATGTC GCAGGAGGAG CTTCTAATGG TGTCTGCCCT 960 TGTCCAGCAT GGTCACCTCT GTTTCCTCTC TGTTCTTTAC TCCTTACTTC TTAATGCATT 1020 TACCTCCCCC ACACCTCCCC CAGACCCCTG CCTTCTCTCT CTCTCATCTG TTTCCCCCCC 1080 TCAGCCTATC TTGTATTCCC CTTTTGCCTT CTCTCCTGAC CTTAGTTCTG CCAAGGACCC 1140 TTCATGGACC TTTAGTGATT AGTCCAACTG TTGCCTGGAA GGTCTAAAGT AGCTGCTAAT 1200 GGTGAGGTTA ATGAATGTAC AGTCACAGGC CAGATCTGGG 1240
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