Tag | Content |
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EnhancerAtlas ID | HS184-19129 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr21:46998130-46999070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GCM1 | MA0646.1 | chr21:46999028-46999039 | GATGCGGGTAC | + | 6.14 | Myod1 | MA0499.1 | chr21:46998419-46998432 | CGCAGCTGTCTCT | + | 6 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAGGTGGGG AAGAAGGTTT GGCATGGCCT GGAAAGTTCC TGAGCCTTCA CTGCCCTTCA 60 GGGAGCCTGG GAGGGGCCTG GGGGACTGGG GCTGGTGTGG TCTCCACTCG GGACCTGCAC 120 GCGCCCCAGG CAGGCAGCGA GGCCAGCAGG CAGAGGTGGG TGAGTGTCCT CGCCGTGTGA 180 CTCTGGCCCG TCCTTAGCCA CGGGGGCTCC TGTGTGGGTA GCTGTCGCAG GCCCACTCCT 240 CCTTTCCGAA CCCCAGAATC GATTTCCTGG TGGAGGTGTG AGGACGCGTC GCAGCTGTCT 300 CTCTCTGAAC CTGCTGCAGG TTCTGGCCCG AGTGCCTGGA TGCCAGACAC CCGCGAGCTC 360 TGCATCAGAC CCGCCTGCCT GGGCAGCCTG GGGCTCACCT CTTGTTTGTC TTTCAACCTG 420 AGCTGGCCCT GAGCCAGTTT GTACAAAGAG TCTGTCGCTT TGATGGGACT TTTCCCTGGC 480 ACTGGCTGGA TGTCCAATCA CCACCCTGCA CCCACATCCC TCCCACTCAG CCTGGAGCTC 540 TGCACTCAAG TGCTGCGTCT TCAGGGTGTC TCTGCCAAAC TCCACTCGAA TCAGGACTCC 600 AGCTGCCACG ATGTGCATTC CCAGCCCTGG TCCCTCCCTG CCCTGACAGG GTTCCCCCCA 660 CCCCGCTCCC AATCCAGACA GGGTTCCCCC CGCCCCGCTC CCAATCCAGA CAGGGTTCCC 720 CCTGCCCCGC TCCCAATCCA GACAGGGTTC CCTCCACCCT GGCCTGCAGT TCCTGGAGAG 780 GAGTGCTTCC GGGGGAGGAG AGGGTCACCT CTTGTGCACA GCACCCCTGG GATGCGGGTG 840 CCCCTGGGAT GCGGGTGGCC CTGGGATGCA GGTACCCCTG GGATGGGGGT GCCCCTGAGA 900 TGCGGGTACC CCTGGGATGC GGTGGCCCTG GGATGGGGGT 940
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