Tag | Content |
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EnhancerAtlas ID | HS006-05636 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr10:104828680-104830150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:104829548-104829567 | GGGTGCCACCTTGTGGCAA | - | 7.17 | POU2F2 | MA0507.1 | chr10:104829241-104829254 | TTAATTTGCATGT | + | 6.5 | ZBTB18 | MA0698.1 | chr10:104829401-104829414 | CAGCCAGATGTGC | + | 6 |
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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 |
GH10I103069 | chr10 | 104829358 | 104830833 |
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Enhancer Sequence | GTAAAGTGGC ACCCAGACCA AGAGACAGGA CGTTACCAGC CCCACAGAAC TCCCATCACG 60 CTCCCTTTTA GTCACTGGTC CCCCAGAGTA ACTGCTTTCT TGACTTCTCA GCCTAATTCT 120 GCCTGCTTTT GAACTTTGCA TAAATGGAGA CACTGTGTGT GTTACACAGA GGCTGGCTCC 180 TTTCTCTGTG TCGTGCTTGT CACATCACCT CTGTTGCTGT GTGTGATCAC ACTATTTCCT 240 CTTGCCATGT CTAGTATGCC ACTGTGTGAA TACACAGCAG TGCACGTGTC CTTTCATTGC 300 TGATAGACAT TGGGGTAGTC CCGTCTGGGG CTACTGTCAA TATGTGGCTT TGAACATTCT 360 TATACATGTC TTTGGGTGAA CGTGTGTGTC CATTTCTGCT GGGTGCGCAC CTGGGACTGG 420 CGCTACGTGT CAGAGGGTGT GCCTCTGGAT TCAGCTCTGA TGTACCTGCT TACTCCCAAC 480 CTGTGCTGTG TGAATTCCGG TTGCTCTGCA TCCAGCACTT GGTATTGTTG AGTCTGTTAA 540 ATGTTAGCAG TTTGGGAGGT CTTAATTTGC ATGTTTCTGA GGACGAATGA GGTTGTTGCT 600 ATATACTGAC TGCCTGTGGC CGGCTCTTGT CTGGAGAGCT GGCCAGGCGA GTCAGCCAGT 660 TAAGGGTGGG TGGCCATGGG GGATTGACAG TTCTCTGAAC ACAAGATTCC AAGATGCCAG 720 CCAGCCAGAT GTGCTCTCAG ACATGAACAC AGATAGATAC CTGGTGGCTT GCTGGCCTCT 780 GGGGATGGCG CTGCTTGGCA GAGCGCACAC GCTTGCTATT AATACCTGAG GCAGCCCGAA 840 CAGGTCGGGC AGGTCGACAG AGATGCTGGG GTGCCACCTT GTGGCAAAAA CACCAAATGA 900 TGTGCGGTTT TAGGAAACTT CATTTACAAA CCTCAAACCT AAAAATAACC CATTTTAAAA 960 GAATTCCTGA AAGCCAGGCT TCCAAGGGGA GGAGATGCCT CCAGACAAGA CTGTTTCTGT 1020 GACATTGGTC TTCATCGACT GCTCCACCCA GTAGTCTGAG GAACCCAAAG ATGTTTCAGT 1080 TAGAAAGTCA CTGAGACGTC AAGAATTCTG TCGTATTTCT AAACTTCCTC TGCCCCAAAT 1140 GCCCCTTCTC ACTATCCTTG TGCAGGTGTT TGAGTCCTGG AGGCACAGTG TCCCCACTGT 1200 CAACTGCTGA CCAACACCCA ACACCCACTG TGAACATGGG CCTGTCTGAC CCTACTTAAT 1260 GAGTAGGTTT CTGTTGTAAA CTTGAAGGTG ACCTTCGTTT TCACTGCTTA GTGAGAGAGA 1320 CAGGGTAGCT CTTACCTAGG CATGAGAAGA CCTGGGTTAT AGCTTCAGTT CCATCACAGG 1380 CAGGTCGTGT GGTGTTGAGC GAGGCCCTTG GTCTCATCCT TGTTAAGAGG ATATAATGAT 1440 GCCAGCTCAT GTGATTATTA GAAGACTAGG 1470
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