Tag | Content |
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EnhancerAtlas ID | HS077-02447 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr12:54566590-54568040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:54566658-54566676 | CTTCCCTTCCTTTCCTCC | - | 6.26 | ZNF263 | MA0528.1 | chr12:54566658-54566679 | CTTCCCTTCCTTTCCTCCTCG | - | 6.14 |
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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 |
GH12I054173 | chr12 | 54566785 | 54567473 |
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Enhancer Sequence | CCGTCTCCCG CTGGGCCTAG GCCCAGCCAG GGTAAGCCCA CCACCTGCTC CCACTCTTCT 60 TAACTTAGCT TCCCTTCCTT TCCTCCTCGG CCCTTTCTAG CTGTTCCCAG TCTGCAGGCC 120 TTCCCCACGG GCACACAGGT GGAGAAAGGC TGAGGACTCA GCGGACAGCC TGGTGTGGTG 180 GGGTCTCTAA GTCATGGGGA GAAGGCAAGG CGGCTTGAAG GGAAGGGTTT GAAGGTGGAA 240 GGATGCAGAA GGCCAGAGAC AAGAAGACGG GAGCAAAGAC AGCCAGAAGC TGTGATGATA 300 CGGTGATACA GAGAGAAGTG GAGGCAGCAT CGGCCAGAAC AAGGGGTCAA AGTCAGAGGC 360 AGAAACAGCA GCGAGAAAAG CAAAAGCTGA CAGATGGCAG AAGCCACAGA CAGGCAGCGC 420 AAGGGAGAGG CAGACACCCA GCGAGAGAGC AAACGGGAGA GGCATCGTGA GACGCGGGAG 480 CAGCTGGAGA GGGAGGTTAG GGCGAGGTGC ATGCACCCCA AGAGATGGAG AAACAGAGAC 540 CAGAGCGAGA GACACGCACG CGGACAGACC AGAAGGCTGC AGAGAGGGCG AGGGAGAAAA 600 AAGTGTCGAG GCGGGGAGTG GCGGGAAGCG GCCGGGAGCG GGGCGGGCGC AGCAGAGCGG 660 GCGCGGCGCC GGGAGCTGGC TCGTAAAAGC CGCGTCGAGC GGGGAAATTA CCGCCAGAAT 720 CGCTGAGCTC CACAAAACGC CGCCCGCGCG GCCCGCCGCC GAGCCCGCTC CAATCTCCAG 780 CCTCATCGCC GCGCGGGCTG GTTATGCATT TAAATGTTAT TTAATTGGAT TGCGGAGGAG 840 CTGGGGGCCA GAGCGGCCGC CCGCCCCCGC CCCGCACGCT CCGCACGCCC GGGCTGCTCG 900 CCTCCTCTGC AAATCTGTTT TCCAAGTCAC AGATTGCAGC ACGCCCCCTC CCAAAACGCT 960 CCCCCCACCC AGACAGCTCC CCTTCGAGTC TGGGCTCCTT CTTCTGTTCC CCCGCCCAAA 1020 CAGAGCCAGA GGACACTCAG AAAGACACGA CAAGCCCCCC GAAGATGCCC CAAACACAGA 1080 GGCTACACAA AAATACCAGA CACACAAAGA CACAACAGCA GCAAAAATGG GTCACACTCA 1140 ATTACACTAG TGTCCATCTG GAAGACTGAA AACTGCAGAG ACAAAAAAGA TCCCATGATC 1200 ACAGGAGGAC ACAAATGCAT GTAATACAGT GGACTCCCAC TCTAGGGGAA CACACTACCC 1260 TACCCCTTAA AACGGTACTT GCAAAGCAGC GCTACCAAAC ACAGGAACAA AATGATGCTA 1320 ACTCAGTGAT TCACAGGGGA CACACAGACC TTCCATACAG CCAGGTAAGG AGCAAAACAC 1380 ATCCACACTC ATGCTCAGAG CAAAGTCATC ACACCCCAAT CACTCAGCTG TGTGGCCTTC 1440 CAGGGTTGAA 1450
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