Tag | Content |
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EnhancerAtlas ID | HS187-05100 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:126175430-126176260 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:126175634-126175646 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr11:126175638-126175650 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr11:126175642-126175654 | GTTTGTTTGTTT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr11:126175534-126175549 | TGAACTCCTGACCTC | - | 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 |
GH11I126305 | chr11 | 126175500 | 126176001 |
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Enhancer Sequence | TCAGCCTCCC AAGTAGCTGG GATTACAGGC ATCTGCCACC ATGCCCAGCT AATTTTCGTA 60 TTTTTAGTAG AGACAGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT CCTGACCTCA 120 GGTGATCCAC CCACCTCTGC CTCCCAAAGT GCTGGGATTA TAGGCATGAG CGACTGCGCT 180 GGGCCTTGTT TTTTGTTGTT TTTTGTTTGT TTGTTTGTTT GTTTTTGTTT CTTGTTTTCT 240 GTTTTTTTGT ATGCGATTCT GTCTGGTTCT CTCAGCCCAG CTGTCTTCAG TGTGCAGCAC 300 CTGTTGAAGG TGTTAGTCAT GAGAGCCTTC GAGCTAGGAG TCACTTGGGA GACCTAGGTT 360 CTGGTTTCTG TTTCAATGCT GACTGTTCAT GTGACCTTGG GCAAGTCACT CAAGGTCTGT 420 TTTTCATCTT CTGAAATGGG GAGAACTTGA CAGAGGTCTT GTAAGCCTAA AATGGAAGAC 480 AACTGAGAAG CCTTGTATTC TGGGGAAGAA AGGTGTGAGA ACTGCCACAA GGATTTGGGT 540 GGAGATGCCT TCTCTGGCTG GGCATGGTGG CTCACACCTG TAATCCCAGC ACTTTGGGAG 600 GCTGAGGCAG GCATATCATT TGAGATCGGG AGTTCAAGAC CAGCCTGGCC AACATGGTGA 660 AACCCCATCT CTACTAAAAA TACAAAAATT AGCCAGATGT GGTGGCATGC GCCTGTAATC 720 CCAGCTACTC AGGAGGCTGT GGCGGGAGAA TTGTTTGAGC CCAGGAGGTG GAGGTTGCAG 780 TGAGCCAAGA TCGCGCCATT GCACTCCAAT CCGGGCAACA GAGCAACACT 830
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