Tag | Content |
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EnhancerAtlas ID | HS017-34053 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr9:134230850-134232340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:134231286-134231298 | AAACAAACAAAC | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr9:134231369-134231384 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 |
GH09I131356 | chr9 | 134231987 | 134232188 |
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Enhancer Sequence | GCTCTTCTAG GTTCCTTTAA ATTGCATATG AATTTAGGAT GGATTCCATA TGAATTTAGG 60 ATAGATTTAG CGATCTGCCC GCCTCAGCCT CTCAAAGTGC TGGGCTTATA GGCATGAGCC 120 ACTGTGCCTG GCCAGGTTGA CTCTACTTTT TAATATGTTC AAAATCGACA TAATGGAGAG 180 TTAGTAAGAA GAAAGTTGGT CAGGTGCGGT GGCTCACACC TATAATCCTA ACACTTTGGG 240 AGGCTGAGGT GGATAGATCA CTTGAGGCCA GGCATTCGAG AATAGCCTGG CCAACATGGT 300 GACACCCCAT CTCTACTAAA AATACAGAAA TTACCTGTAG TCCCAGCTAC CTGGGAGGCT 360 GAGGCAGGAG AATCACTTGA ACCTGGGAGG CGGAGGTTGC AGCGAGCCAA GATCGTGCCA 420 TTGCACTCCG TCTCAAAAAC AAACAAACAA AACCAGGCTG GGGGTGGTGG CTCATGCCTG 480 TTATCCCAGA ACTTTGGGAG GCTGAGACAG GTGGATCACG AGGTCAGGAG TTCAAGATCA 540 ACCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG CTGGGCGTGG 600 TGGTGGGCGC CTGTAATCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATT GCTTGAACTT 660 GGGAGGCAGA GGCTGCAGTG AGCGAAGATC GCGCCACTGC ACTCCAGCCT GGATGACTCC 720 ATCTCAAAAA AAAAGGCCAA GTGTGGTGGC TCACACCTGT AATCCCGGCA CTTTGGGAGG 780 CCGAGGTGGG TGGATCACCT GAAGTCAGGA GTTTGAGACC AGCCTGACCA ACATAGTGAA 840 ACCTCATCTC TACTAAAAAT ACAAAATTAG CTGGGTGTGG TGGCACATGC CTGTAGTTCC 900 AGCTACTTGG GAGGCTGAGG CAGGAGAATG ACTTGAACCT GGGAGGTGGA AGTTGCAGTG 960 AGCAAAAGTC ACACCATTGC ACTCCAGCCT GGGCAATAAG AGAGAAACTC CATCTCAAAA 1020 AAAAAAAAAA AAAAAAAAAA GAAGAGCTCA TGTCATCCGC AAATAGAGAC AGTTTTACTT 1080 CCTTCCCAAT GTGGATGCCT TTTACTTCCC TTTCTTGCCT AATTGTTCTG GCGAGAACGT 1140 CCAGTGCACT GCTGATAGAA GTGACCAGAG CAGGCATCCT TGGGTTGTTT CTGCAGAGGC 1200 TGAACTTTTA ACCGCATGAT GGACTTTTTC TGCTGAGTCG TCCTGATTCT TGGTTTGTGG 1260 GGAAAAGCAA GAGAGATCAG ATTGTTACTG TGTCTGTGTA GAAAGAAGTA GACATAGGAG 1320 ACTCCATTTT GTTATGTACT AAGAAAAATT CTTCTGCCTT GAGATTCTGT GACCTTACCC 1380 CCAACCCCGT GCTCTCTGAA ACATGTGCTG TGTCAACTCA GAGTTGAATG GATTAAGGGC 1440 GGTGCAAGAT GTGCTTTGTT AAACAGATGC TTGAAGGCAG CATGCTCCTT 1490
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