Tag | Content |
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EnhancerAtlas ID | HS127-32602 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr9:134230820-134232290 |
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 | CTTTATTATT CTTTTTCAAG ATCATTTTTG GCTCTTCTAG GTTCCTTTAA ATTGCATATG 60 AATTTAGGAT GGATTCCATA TGAATTTAGG ATAGATTTAG CGATCTGCCC GCCTCAGCCT 120 CTCAAAGTGC TGGGCTTATA GGCATGAGCC ACTGTGCCTG GCCAGGTTGA CTCTACTTTT 180 TAATATGTTC AAAATCGACA TAATGGAGAG TTAGTAAGAA GAAAGTTGGT CAGGTGCGGT 240 GGCTCACACC TATAATCCTA ACACTTTGGG AGGCTGAGGT GGATAGATCA CTTGAGGCCA 300 GGCATTCGAG AATAGCCTGG CCAACATGGT GACACCCCAT CTCTACTAAA AATACAGAAA 360 TTACCTGTAG TCCCAGCTAC CTGGGAGGCT GAGGCAGGAG AATCACTTGA ACCTGGGAGG 420 CGGAGGTTGC AGCGAGCCAA GATCGTGCCA TTGCACTCCG TCTCAAAAAC AAACAAACAA 480 AACCAGGCTG GGGGTGGTGG CTCATGCCTG TTATCCCAGA ACTTTGGGAG GCTGAGACAG 540 GTGGATCACG AGGTCAGGAG TTCAAGATCA ACCTGGCCAA CATGGTGAAA CCCCATCTCT 600 ACTAAAAATA CAAAAATTAG CTGGGCGTGG TGGTGGGCGC CTGTAATCCC AGCTACTCGG 660 GAGGCTGAGG CAGGAGAATT GCTTGAACTT GGGAGGCAGA GGCTGCAGTG AGCGAAGATC 720 GCGCCACTGC ACTCCAGCCT GGATGACTCC ATCTCAAAAA AAAAGGCCAA GTGTGGTGGC 780 TCACACCTGT AATCCCGGCA CTTTGGGAGG CCGAGGTGGG TGGATCACCT GAAGTCAGGA 840 GTTTGAGACC AGCCTGACCA ACATAGTGAA ACCTCATCTC TACTAAAAAT ACAAAATTAG 900 CTGGGTGTGG TGGCACATGC CTGTAGTTCC AGCTACTTGG GAGGCTGAGG CAGGAGAATG 960 ACTTGAACCT GGGAGGTGGA AGTTGCAGTG AGCAAAAGTC ACACCATTGC ACTCCAGCCT 1020 GGGCAATAAG AGAGAAACTC CATCTCAAAA AAAAAAAAAA AAAAAAAAAA GAAGAGCTCA 1080 TGTCATCCGC AAATAGAGAC AGTTTTACTT CCTTCCCAAT GTGGATGCCT TTTACTTCCC 1140 TTTCTTGCCT AATTGTTCTG GCGAGAACGT CCAGTGCACT GCTGATAGAA GTGACCAGAG 1200 CAGGCATCCT TGGGTTGTTT CTGCAGAGGC TGAACTTTTA ACCGCATGAT GGACTTTTTC 1260 TGCTGAGTCG TCCTGATTCT TGGTTTGTGG GGAAAAGCAA GAGAGATCAG ATTGTTACTG 1320 TGTCTGTGTA GAAAGAAGTA GACATAGGAG ACTCCATTTT GTTATGTACT AAGAAAAATT 1380 CTTCTGCCTT GAGATTCTGT GACCTTACCC CCAACCCCGT GCTCTCTGAA ACATGTGCTG 1440 TGTCAACTCA GAGTTGAATG GATTAAGGGC 1470
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