Tag | Content |
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EnhancerAtlas ID | HS182-08078 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr16:15752620-15753610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:15752732-15752747 | TGAACTCTTGACCTC | - | 7.64 | RARA | MA0729.1 | chr16:15752729-15752747 | TCTTGAACTCTTGACCTC | - | 6.45 |
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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 |
GH16I015658 | chr16 | 15751911 | 15755196 |
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Enhancer Sequence | CTCATGCCTT AGCCTCCCGA GTAGTTGGGA TCATAGGTGC CTGCCACCAC ACCCAGCTAA 60 TTTTTGTGCT TTTAGTGTAG ACAGGATTTT ACCATGTTGG CCAAGCTTGT CTTGAACTCT 120 TGACCTCAAG TCATCTGCCT GCCTCAGCTT CCCAAAGTGT TGAGATTACA GGCATGAGCC 180 ACCACGTCTG GCCAGCTTTG TATGACATTT CGCCTTTCTG CCTTGATCAA ACTTTCAGAG 240 AATCTGCTTT CCAGAGGGAT GAGTGGGTCG GGAAATAGCA TGTTTTCTCT GAATGAGGGA 300 AAGGATTGAA AAAGTAGGAG GGAGAAAGGA TGTGAATATG AGTCCCAACA AATGCAGAGT 360 TATCGGTAAG TTTTGTGCTT GAATCTAGGT ACAATTGTGC ATTTCCTGGT TCTGCATGAA 420 TTAGGCCCAC CTCTGTCATT GGCTCAACAT GGGTGAGGCT CACTAACTTC CACCAGAAGT 480 TAGTGGTGGT GTCTGTGTTG ACACTTACAT GTTTAGCCTA ATGATTTCAT GTTTTAACCA 540 AAACTATATA GCTTGTTGGT TATATCTTAG AAAGTGATGG TTTTTGCTCA TTCTTTTGTC 600 CCCAGGGATA CACACCAGCC TCTAAGTTCT CTTGAGGGAA GGAAGGGACC TTGCACACAA 660 TCTTTTTTTT TTTTTTTTTT TTTTTTTTTT TGAGAGGAAG TCTCACTCTG TCACCCAGGC 720 TGGAGTGCAG TGGTGCGATC TCGGCTCACT ACAACCTCTG CCTTCTGGGT TCAAGTGATT 780 CTCCCGCCTC AGCCTCCCGA GTAGTGGGGA TTACAGGCGC ACACCACCAT GCCCGGCTAA 840 TTTTTATATT TTTAGTAGAG ATGGGGTTTC AGTGTGTTGG CCAGGCTGGT TTCAGACTCC 900 TGAGCTCAGG TGATTCACCT GCCCTGGCCT CCCAAAGTAC TGGGATTACA GGTGTGAGCC 960 ACTGCGCCCG GCCTTGGACA CAATCTTTTT 990
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