Tag | Content |
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EnhancerAtlas ID | HS105-57522 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr3:133569740-133571310 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP4 | MA0685.1 | chr3:133570517-133570534 | AAGGGGGGAGTGGCTTG | - | 6.04 | TBX20 | MA0689.1 | chr3:133570152-133570163 | GAGGTGTGAAG | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTGACAGTA GCCAGAGGAA AATGACACAC CTCACGCAAG GAAATAACAG GGATGACGGC 60 TGCCATACTG GAAAAAAATG GAAGCTAGAA AACACTGGAA TGACACAATA AAAGTGTTCA 120 AGAAAAAAAA AAAAAACCGT GGAAACAGAA TTCTAAATCC AGCAAAAATA CTCTTCAAAA 180 GTATGAAGAA ATAAAAATAT TTTTAGATAA ACAAAAACAA AGAGAATTTG TGGCAAGCAG 240 AACTTCACTA CAAGAAATGT TAAAGGAAGC TGTTCAGGCT GACAGGAAAA TATACTAATG 300 GAAACTAGAA TTCTCTGGAA GAAATTGTGA GCATCAGAAA TGGTAAATAC ATGCATGGGT 360 CAATGCAGGA CATTGTTTGT TTTAGATAAA AGTGATGGCT TCAGTACACC CTGAGGTGTG 420 AAGCCACACA GTTTCTTCAG AAAAACAAAA ATGATTCAGG ACCAATGGAC TGTGAATTGC 480 CTGTAGAGAA CAGGATGGAG CCAAAGAACT GATAAACGAC CAAAGAAGAG GGACTTCCAT 540 GTAGCTGGGG CTTTAGAAAG ATAACCCTGG TTGAAGGATA GTGAATGGGA TAAAGGCAAG 600 GGAGACAAAA CGGAACCTGC TGCAAAGGCC TAGACAGGCA AAGAGGTGTG GGCAGAGAAG 660 AGCAGAGTGA GAAGGAAGGA GGACACATGA GTGATATCAA GAAGCAGAGG CAGGACTCCA 720 TGGGTGTGAA AGATGTAGAG AGGCTGGGTG ACTAAGATAA GGTACTGTTA ACAAGAAAAG 780 GGGGGAGTGG CTTGCACGAC TGGGAACACT AACTACACTT TGCAGATAAG CCAGAGCCAC 840 ACAGAAGTGA AGTGACTTGC CTGAGGTCCC ATAGCAAGTC AGCGAGGTCA CAGGAACTAA 900 TTTGCATCTT CTCTGATGAT AAATCATGGG CTTTGGGTGA TGAAATAAAA GACGACCTTC 960 ATGGGCTGAC TCCTTTGGAG CACATCCCAG CTAGGGTAGC CACTAAAGGA TGGCCCAAGG 1020 TGCTGCTTCT CTGGAAGCAA CTGCAACCAC ACCACTAGAA CTAATGAGAA ACGACCACAC 1080 TTGGGTGTCA TTCATGCCAC CTCCATGGAG AGCCACAAAG TTAGATCTAC ACTGATGGGC 1140 ATTCTCCTCG TCACAGGGAA TGAGCGTGGT CCAGGCGTGG TTTTGCGAGG CAGCTGGGCT 1200 TACCAGCCAA TACAAGATTG CCAAGCATCA AAGCCAATGG TGCTCCTGGG ATTCCCGGGG 1260 CTGCGGGGCT CTGTCTAAGA GCTGTGTCTA CCACTGTTCT GCTGGGTACT CTAGTCTCAG 1320 ACTTGTGCCA AATCAGATCC TCAGAGACCA CGGGCCTAGG CTGCTTTGTC CACACTCTCC 1380 AGGATGGTTT TAGCAGCAAG TAAGCCAGAT TATGCTGGCA TTGCACTTTG GAGGTCTGTG 1440 AGGGTCTGTA TCACAAATCA TCATGTGAGG AAAGTCTCTA TCTTGCTGGT AACACTGTCA 1500 CTAGATGCCC TACCTGCCAA GCCATTACAT ATACCTCTTT GTAAGCTGGG GCAGAGAAAC 1560 CCTGATTTTT 1570
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