Tag | Content |
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EnhancerAtlas ID | HS184-12035 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr16:8779610-8780590 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr16:8779619-8779640 | GGATGAGGAGTGGCAAGAGGA | + | 6.46 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 8779620 | 8779767 | chr16 | 8779800 | 8780226 |
| | Number: 1 | ID | Chromosome | Start | End |
GH16I008686 | chr16 | 8780027 | 8780268 |
| Enhancer Sequence | GGCATGGGTG GATGAGGAGT GGCAAGAGGA GGCTGTAGGA AGAGTAGATC ATGTCCCGCC 60 AGGTGACCCA TGATCTTGAA TTTGGACTTG ACTCAGAGAC CCATAGGGAA CCATGGAAGA 120 GATTAAAGCA AGGCAGTGAT GTGATTTTGT TATCACTTGA GAAAGATCCT CCTGGAAGCT 180 GAATGGAGAG TAGACAGACA CCTTCTCCCA CTAGCCTTTG AGCTCAGATT TCCTTAGGGA 240 AACAGCCAAT CCCAGGGGCA GATTGCTGAC CTTCCTGCAA AAGGTTTTAG AACGTGGAAG 300 CTCCTTCAGG GCAAGGTTGG CTGAACACCA GCCAAAAGAG CAAGGCACCA CCCCGGCAGG 360 ACAGGGCTGT TTTGTGCACG GGAACAAAGC CTGCCTCCTC TCTCTGCCCA GAGCTGTAAA 420 TAGCACTCTG CTGGCTTCGC AGGCTGAGCG CCGGTCTGGG GACAGGCTGA AAATGCACAC 480 ACCAAGGAGC ATTTGTGCAA ATGAATGCCT GCATGCAAAT TTGCATGCCT GGCATCCTGC 540 CCCAGCCCTA AGTGTCCAGT CCTGCAAGGG GCTGGAAGCA GGGCTCAAAA AAGAGCCACA 600 CACAGAAGAG TGTGGACATT CTGACCTGGG GACAGGTTCC AGGAGGGATT CAGAGGCAGG 660 CTGGCAGGGT GAGTGGGAGA AAACATGCAG AGAACCCTGG ACAGAGTTTT GGCTCCAGCT 720 TTACCCATGA TAATGACAAT GACCCATGAG TAGTAGCCAC TCACATTGGC TGTGTATTTG 780 TGTGTAGTTG CTCACCTTGT CGCTCACAAC AGCCCTATGA GGAAAGGCTG ATCAGATTTC 840 AGAGACAGGA AATGGAAACT CAGAAAGGAT GACTGACTCG CCCAGGGTCT CCTACTGAAG 900 GGAGCATTTC TAGTGAGAAA CCGAGGCTTG AAGACTCTGG AGCCCTGGTG TCTAGGACTG 960 ACCCACATGG ACGCCTCTGC 980
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