Tag | Content |
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EnhancerAtlas ID | HS060-11110 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr15:40569690-40571330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr15:40569859-40569880 | GAAGGGAAACAGGAAGTGAAA | - | 6.04 | ZNF263 | MA0528.1 | chr15:40569843-40569864 | AAAGGAGGGCAGAGAGGAAGG | + | 6.56 |
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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 |
GH15I040277 | chr15 | 40569602 | 40570401 |
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Enhancer Sequence | GGGCTTCCTG TGTCTCTGGG AGCGGAGACC GGCCGTCTTG GAGGGGGGTC TCCTGTGGCG 60 GGTGAATCTC GTGTAGCCTC CCCTCCTCCC CACGTGAGCT CTCCAGCAGC CACACCACAG 120 AACACCCAAC TTCCCTGGTG GCCTGTGGAC CCGAAAGGAG GGCAGAGAGG AAGGGAAACA 180 GGAAGTGAAA GGCCCTTGGG AATGAAGGCG ATGAAAAATA GACGGGGCTA CTTCCCCAGG 240 GGAGAAGAGC CCACAAGGAA AGCCAGGGCC CTGCGCTGCG TTTGCGGGGG GTGGCCGAAG 300 TGGCTGACGA CCACCCTGTG TGTCAGCTTC TCCCATCCTC TGCGCGCTCC TCACCCCCAC 360 CCCAGACCTC CAGCTGTCCA TAGGAAGTGG TCTGAAACCG CTTCCAGTGG GAGAGCAGTC 420 CCTGCCTCAC TCCTCAGGAC TGAGGGAGAT GGTGTGGGGT TCAAAAAGAA CGGAGCAGAG 480 CCTGGAAACC AGGGAGCCTG GGCTTTCGTT CTGGGGGTGG GGAGGTGGAT GAAATTATCT 540 TGCAACTTCC AGCTCCCACA CGGATTCCCG CACTTCCTTC CTGAGATCTC CCACTGCCCA 600 GGATTCAGGA GCAAGCCAGG AGCAAGGAAC CATGCAGCCT TTCTTTCACT CCCCAGTGCA 660 TTCACACCCT GACAGGTGCC CTGGTGCTGC GGCTGGCCCG GCCTGTCCCC CCAGCTCAGC 720 AGAAGCAGCA CCTGTGACTT ACCTTCAGGA GCCAGCACAG TAGGACGGGC AGGGCGGAGG 780 CTCACTAAGG CAGGGGCCTC CACAGGAGGC AAAGGCTCGG TCCATCTCTC CAAAGGGAGC 840 CGAGGGTCAG GAGTGCTTGA TAAGGCAAAG AGAGGCCAGT TCTCGCAACG GAATAATACA 900 CTGGATTTAT TAACTATTCT TTGAGTTCTA ACAGTCCTTC CACCACACAG TATCACTCTG 960 AAAGGGTGTG CATGTCTCAC AGCTCACACA CACACCACTT CTGATCTTAG GGTACCAAGT 1020 GCCAGCATCC TGGGTGACTC TTCACAATGA CAAAAGCAAC AAGAACTGGA AAAGCAAAAT 1080 ATTTAGAAAA GTCTCTTCTG AAGGTAGAGA TTGCTAGAGA GGACCCAGCC TCAACACCCT 1140 GGGGCTGACA AAGGGAGTTC AGGAGAGAAA AATGTGGTAA AACATGGAAG TTCTGCACAG 1200 AGCCGGGCCT GGGAAGGAGT CTGTATGTAT GGACAGCAAG GCAGTCAGAC ACACGATGCA 1260 GTTCAGACAG GAAAGAGCCG CTGCAGTTGT TTAGAAACAT CGCTTTCTAC CACCAAGCTC 1320 TCGGCAGCTC CACAGAGAAG AGCCCTCATG GTTGTTTATC CAGTCAAGAG GGCCCAGGGT 1380 GACATTCAAC CAGAAAGCCG TATATCAGAG ATACTGGAAA GATTACAGCA CCTCTGATAC 1440 AATGTGCAAC CCAGACTTCA TGCTGTTAAG CCAAAATACT TGCATTTCTA CACCACTAAA 1500 AACGTCATTA AAATTCAACA CAGTTGAAAA GGGAGTACAT AAGCAAGCAA GGGTCAGAAA 1560 GCAGCAGTTT GCACTTGGGG TGTCCAGTGG TCCCCACCCT ACCCCAGACC CTCTCTCTCA 1620 GGCTTTTCAG GCACTTGGTA 1640
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