Tag | Content |
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EnhancerAtlas ID | HS006-08364 | Organism | Homo sapiens | Tissue/cell | Astrocyte | Coordinate | chr12:1057130-1058760 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr12:1058532-1058542 | GGTGCCAAGT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGAGTTAAA TGCTAGTTTC CAAAAACTTA AGTTTTAAAT GTCTGTGCCT CAGACTGCGA 60 GTTCTGTGGA GGACTAGACC TAGAAAGCCT AGAAAATCAC CAGTATCCAT CAAAAATGGA 120 GAAACAAAAT GTGGTATATC CACACAATAA ATAATTCAGT TATTTAAAAA ATGAAGTTGA 180 TACATGCTAC ATACAACATA GATGGACTTT GAATCATGAA GTGAAATAAA CCAAACACAA 240 AAGAACAAAT ATTGTATAAT ACAGTACTGA GAATGGGTAA ATTCATAGAT TAGTGCTGCT 300 GGGAGTAGGA GGAAATAATG GGTGTCTGCT AATGGTTTTA AGGTTTCTTT TAGGGATGAT 360 AAAAATGTTC TGGAATTAGA TAATAGTGGT GATTGCACAA CCTTGTGAAT ATATTAAAAC 420 CACTGAATTG CACACTTTAA AAGGGTGAAT TTAGACTGGG TGTGGTGGCT CACACCTGTA 480 ATCCCTGAAC TTTGGAAGGG CGAGGAGTTC GAGACCAGCC TAACCAACAT GGTGAAAAAT 540 ACAAAGTAGC TGGGTGTGGT GGTATGCGCC TGTAATTCCA GCTACTTGAG AGGCTGAAGC 600 AAAGAATCGC TTGAACCCAG GAGGCGGACG TTGCAGTGAG CCGAGACGGC GCCACTGTAC 660 TCCAGCCTGG GCAACAGAGC GAGACTATGT CTCCACTTTT TTTTAAAAAA GGGAGTGAAT 720 TTAATTGTAC GTGAATTATA ACTTTTTTTT TTTTGGATGG ATTCTCGCTC TGTCCCCCAG 780 GCTGGAGTGC AGTGGTGCGA TGTCGGCTTA CCGGCACACC TGCCTACTGG GTTCAAGCGA 840 TTCTCATGCC TCCGCCTCCC GAGTAGCGGG GATTACAGGC GCCCGCCACC AGGCCTGCCT 900 AGTTTTGTAT TTTTAGTAGA GACGGGGTTT CGCTATGTTA GCCAGGCTGG CGTAGAACTC 960 CTGGCCTCAA GCGATCCTCC CGCATCGGCC TTCCAAAGTT CTGGGATTAC AGGTGTGAGA 1020 CGCCGCGCCA GACCTCTATC TCAATGTTAT AACAAGGCTC AATACTCAGC TAAAGTGAGC 1080 GTCAAATTTT TATTTTTATT TTTTCCCCCG TGACAGGGTC TCGCTCTGTC GCCCGGGACG 1140 GAGTGTCGTG GTACGGGTGC GATCTCGGCT CACTGCAGGC TTGACCTCCA GGGAACATGG 1200 GGGCATGCCG CCACCATGCC CGGCGTCAAA TTCCTTTTAA ATCAATCATT TCTTCCCAGC 1260 GTCCCCCGCT CCCTGCAACT CAACTTCGTT TAGCTATTAA CACAAACTTC AGATTCCCCA 1320 CGCCTGTCTG CAGGCAGCAT CTCCAAGGAA GCGCCACCAC GGACACCTGG CTGTCCGCAC 1380 CGCGGTGGGG TCCCGGCGCG TTGGTGCCAA GTTTCCTGTA CCCCGCCTTC CTACCCACCT 1440 CTCGGGAGGC CCGGATACTG AGCCCCTCAC TGCACTGGTG AACTAGAACA GGCCTCTGGA 1500 CTCAGCATCT CTACGCTGAG ACCTCAGGAT CAGGTCCACC GCAGCCCCAG GTTCTCGACC 1560 CGGAAGCTGA GCCTTCCCAC GCTCCACACC CACGGCTAGA ACCACCCCGG GGGAAGCCGC 1620 TCTCCTCCCC 1630
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