Tag | Content |
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EnhancerAtlas ID | HS184-13431 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:37747830-37749220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr17:37748772-37748793 | GTCTCTGTCCGTGGTGCTGAA | - | 9.62 | ZNF263 | MA0528.1 | chr17:37748990-37749011 | AGAGGAAGAAGAGGATGGAAG | + | 6.25 | ZNF263 | MA0528.1 | chr17:37748892-37748913 | GGAGAAAGAAGAGAGGGGAGA | + | 6.49 | ZNF263 | MA0528.1 | chr17:37748889-37748910 | GGAGGAGAAAGAAGAGAGGGG | + | 7.67 |
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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 |
GH17I039592 | chr17 | 37748701 | 37748850 |
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Enhancer Sequence | CACCCCTGAT GACAACTCCA GGGCCTGCCC TTTGCTGGGG AAATGTGACC ATTTCTTGGG 60 GAGGGCACAG CTCTCACAAG ACTTACCAGA CCCTTAGAGC AGTTGCCTGG TGTCATAGGA 120 GGTAGGTTCC CATCTGTGTA GTGCAGGATC CTGCTCTGTG ATACAAAAGG CTGATTCTTG 180 TATTCATCCT CTGAGGATGG CTTTGGTGTT TGTGCAGGTG CATTTACCCT TCTGTATATG 240 TGTGTGTGCA TTTGTGTAAT AATTGGTGTG CAAAGGACCA GGTGATTTGC ACACATGCAT 300 GCAAGTCAGA ACAGCCTGGA TTCTGTGCAT TTCTCTCAGG ATATGTGTGT GTGAAGGGAT 360 GATTATCTGG TTGTCTGGGG CCTCAGAAAG GCAGGTAACT TGTAAATTTC CTCAAGCATG 420 TGCTGGTGGG TGGAGTTCCC ACAGGATGGA AAAAGGGGCT GGCCCCAGAG TTGAGTTCTG 480 AGCTCAGCTC TCCACCTCTT CCTGCCCGTC TCCAGCTCGC TGCCTCCCCC TACTTTTCCC 540 CAAGCTGGGC AGAATGCCCT CAGCCTGTGC CGGCTGGCAC ACATGCCACA TGGTGCCTGG 600 CGCGCGTCTG GGCAAGGATG ACGCCCCCAG GACCGGCTGG GATACCAAGC CACCCGCTGC 660 CTCCCCCACC TCCAGAACGG AGCGTCCCCA TCCCATCCCC TTTCCCAGCC AGGGACTCGG 720 GGAGCAGGCA GGGACACAGC ACAGACAGAT ACAAACACAC AGATGCACCC AGAGACGCCC 780 ACAGGCGTGT GCCCCAGAGG GACACAGACA CAGGCGTTCA CACAGGCTCG GGTACACACA 840 CGCACGCTCA CACCCCCCCA GAGAAATTTA TGAGTGGTCA CCACTTGCAC GGATCCAGAC 900 AGAACCTGAC CCGCCTAGGA CATTTAGGCA AATCCACCTG GTGTCTCTGT CCGTGGTGCT 960 GAAACAAGAA TGTTTGAACG TCCTCCCTAT GGAAGCACTA ACAGGAAGTA GAAGGGAGAA 1020 AAAGACCTGG GAATGGGTGG TGGACAAAAA AGAAGCAATG GAGGAGAAAG AAGAGAGGGG 1080 AGAGAGAAAT CTGGTGGTAA GGGAGATAGA ATGTAAAGGA TTCCAGGAGG ACCAAGGACT 1140 GTCTGAACCC TGGGACTAGG AGAGGAAGAA GAGGATGGAA GATGATCTCA GCCCCATCCC 1200 TGTCCCCTGA ATGTGTGGCT CCTGTGGCCT CCAGTTACTC CTTCCATATG CCACCTTGCC 1260 CTAGATGACC TGAAAATAGT AGGGAAAGGA GATGGACCTG GGAAAGCCCT ATAGTGGACC 1320 TGCAGATAGC TCCCTACCTG ATTACTTATC TCAATTTGTG TTGGGCAAGT GGACAACACT 1380 GTTGATCTGG 1390
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