Tag | Content |
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EnhancerAtlas ID | HS089-13123 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr9:136545850-136547490 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr9:136546249-136546270 | CTCAGCACCGGGGACATCTGC | + | 6.39 | ZNF263 | MA0528.1 | chr9:136545954-136545975 | GGAGGACAAGGAGGGAGAGGG | + | 6.91 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 136546231 | 136546312 | chr9 | 136546377 | 136546595 | chr9 | 136546665 | 136547008 |
| Enhancer Sequence | TCCTCCAGAC ACACGCAGAC CTGGCCGCCA GGCCCACACT GGCCACTCCA GACACACGCA 60 GACCTGGCCG CCAGGCCCAC ACTGGCCACT CCAGAGAGCT GCCGGGAGGA CAAGGAGGGA 120 GAGGGACGAG AAGCCAGTGG GGCTGCGCTC AGTGCTGGGC ATCAGGGTCT CTAGGTGAAG 180 ATGGTTAGCC CCAGCTCACC CCCAGTCTGT CCCCGATGGA CCCCACGGAC TCCAAGAACA 240 TGAGCATGGG AATGACCCCA CAGAGCCGGC CACTCAGCCC AGGTGACAGT AAATCTGTGC 300 GCTAAGGTCG TCTGTCTTCC TAAGGAGTGG GGCCCTGGGC CACTGGCTGT CGGCAGAGAC 360 GAGCTCCTGG CTGGGGCTGT GTGGGGATGG AAGCCTGCCC TCAGCACCGG GGACATCTGC 420 CGCCCTGGTC CTGCCACGGG GGCTGGGAGG TGTCAGGATG GGGCCCACAG GGATGGGGAG 480 AATGCTGGTG GGTAGTGGGT AGAGCAGGGG CAGCTGATGT GGGCTCCCGG CTCGTCCACA 540 GGCCCCTGGG GTCAGTCCCA GGGCAGAGCC CCCCAACACG GGCCACACTT TTTTTCTAGC 600 CAAGAGGTCG AGACACTCGG GGCCTTGCCC CACCCTGTCT GGTTCTTGCC AACACTCAGT 660 TCTCTGTGGC CATCTTTGCG GGACTCTCGG TTCCATGAGA ACCCGTTGGC CTGGGGTCAC 720 CCCTCACCCT GCCTAGGACC TCTTTCCAGT ACAGGCTGGG CTGTGGCTGC AGGTCCCTTC 780 CTGGGCCCCA ACCTCACTCG GGGTCTGAGC CCATCGAGGG AAGGAGCCAC ATCTTCCATC 840 CTGGGACCCC AATCCAGCAC CCAGCAGGCT CCCAGGCAGC ATGTCCAGAG TTCACTCCAG 900 AGTCTCTCGA GCGCTAGTGA GGGAGAGGAC GAGAAGCACA GCACTGGGAA CGGATCGTTA 960 AGTTTAGTAA AACACTAGTG CTTGACTGAG AGTCCCAGTG GCCCTACGTG AGCTGACGGT 1020 GCTGGGAGGT ACACCATGGA TAACTGCCAC GGCCGGTGCG CGGCGTGTTT CCCAGCAGCT 1080 GGGCCTCCTT ATGCGTGTAG CACCTCCCCG CCGCCTATTT CCTGTGTCCC CACGATCGCG 1140 CACGCCAGTT GACGCTCATG TCCCACCTCC CCTGTGTTTC CCCTCCCCCC CATCCCACAC 1200 GCAGGGACCC CAGCCTAGAA AGCATTGTGC TTCTCTCCCA CTCCGCCTGA GACCTAGGGT 1260 AGCACTGGGC AAGCGAGGGG CGCAGAAATA CGGAAGGACA GAGAAGAACA CACCACAGAG 1320 TGACCCGGGA CCATGAACCG CACATACCTC CGACCTGGTG GGCCCAGCTC TACCCTCTCT 1380 CAGACCAACA GTCAGCATCT ACTGGGAGGA CGGTGTTCAA GGGAAGTTCC TCCCGGGGCC 1440 ACTTCCAAAG CAGAGAGGTG GACCCGGTGT GAAACACATG AGCAGGGCAC TGGAGACGCA 1500 GCTGAGGGCG TTCCAAGTGG TTCTCGGGGA ACGTTCAAAG GAACAGGGGA ACAGTCACGA 1560 CATTCGGAGA ATAAAGCAGT GTGTACAGAC TGCATGGGAT GCCCTGATTA CATTTTAAAA 1620 TCCACAGATA GTCACAGATG 1640
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