Tag | Content |
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EnhancerAtlas ID | HS183-02521 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr17:76986120-76987790 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr17:76987734-76987745 | TGCGCAGGCGC | - | 6.62 | ZNF263 | MA0528.1 | chr17:76987065-76987086 | GGAGGAGGCGGGGAAGGAGAG | + | 8.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCACTTGAGA TCAGGAGTTT GAGACCAGCC TGGCCAATAT GGAGAAACCC CATCTCTACT 60 AAAAACACAA AAATTAGCCG GGCGTGGTGG CGCACGCCTG TAATCCCAGC TACTTGGGAG 120 GCTGAGGCAG AAGAATTGCT TGAACCTGGG AGATGGAGGT TACAGTGAGC CAAGATCGTG 180 TCCCTGCACT TCAGCCTGGG AGACAGAGCA AGACTCCATC CCCCCAAAAT AAAAAAAAGA 240 AAAGAAAAAA AGTATACTGG AATACAGGAT TAACACGTGG AATGAAAGAA ACTGAATCTC 300 GTTTTTTTGT CCAGTTGAGG TGACTGGAGA GTCTTCCATT TGCAGATGAG CTGTGTGCCG 360 GACCCATGAG TGTGGAGCCG GCAGTCACTG CCCCACGAGT CCCGCATGTC ACAGCTTCTT 420 AAACAGATGG TCAAGAGCTT ACATGCGGTT CCTTATCCCA ACCCGCCGCG GCCCGATGCG 480 CCCTGGCTTT TTCTGGAACT GTTGTTCTGT GGATCCTCGC CGAGAACGCC CAGTTCTCCT 540 TGCTGCTCAG TCATGGAGTC TCTCTGGGGA CCCCGCTGCC GCGCTGGTCC TTCTGCAGAG 600 GCCGCCTCCC TGCAGCGCTG TCTTGGTCAG GCTCCCAGCA GGAAAAGACG ACACCCGAAT 660 GAAGATCATC TAAGGAGGCT TCAGTGAAGG GACCATTTAC CACGGATGAG ACAGCAGGGC 720 GTGCGGGCGG CACGAGGGGC CGCTGTAGCA TCTGGAGCTG CTAACAGTGG AGCTGTCACT 780 CCCATGTCAC ACTCCCAGGC CAGAAGAGAC CAGGGGAGGG GACTCAGCCC AGACACTGGG 840 AGTGGCACCA GGGGGCTGCC TTGAGAGGCG AGTGCCAGAG AGAGTCAGGG ACTCCCCAGG 900 GGCCATCCCA GAGGGCACTG AGGAGGTTCA CTGGGTCTGG GACCCGGAGG AGGCGGGGAA 960 GGAGAGTGGG TCTGAAGGGT AAGGGGTCGA TGTGGGTGCA ATTGCCCTTT CTGATTCCGC 1020 TCTCCCGGTT TTCTGTCCCT CTCTGGCCGC CCCTGTCCTG TCTCTAGTTG AGGTCTTTCT 1080 TGGCCAGTGC CTGCCTCCCT GGCGCCTGTG GTTTCAGTGA TGGGGATTCT TCCATGCGTC 1140 ACTTGGAGCG ACCTCGTCTG TTCCTGTGGA CTCACTGACA CACTAAAGAC ACCAGCTCAG 1200 CCCTGACCTC TCACCTGAGC GCCTCCTTAC CAAGTCATCC AGATGGCTCC CCAGGGATGA 1260 GCAGCAACAA AACGGGCACG TGGGTGCCCA GCACACGTCA GGTGATGTTC TAAGCCCCTT 1320 GCGCGTACCC AGTCACTTAC CGTTCACTGC AGCCCCGGGA TGAGCTCTGC GATGAGCATC 1380 CTTTTGCAGA CGAGGACACT GAAGCACAGG AAAGTTAGGT CATTTGCCTA AGGACATGCA 1440 GCTGGATGGG GACAGAGCCA GGATCGGGCT TGCAGTGGCT TCAGACCCCA CCTTTCTGAC 1500 CACAGCGCTC GTGCTCTTGG AGCGCCTTGA GATAGTGGGA CAAGGCGGAC TGGAGGACGC 1560 AGTTTCCAGA TGGGATGCCC TGGCGGGCGA CTCCCGTGCG CATGCCCAGC ATCCTGCGCA 1620 GGCGCTCTCG TGGCCAGGCC TCTGCAAACA GTCAGCACAG ACCGGGAGAC 1670
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