Tag | Content |
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EnhancerAtlas ID | HS176-15971 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:16186460-16187440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr17:16186926-16186941 | GAGTTCAAGGTCAGC | + | 8.73 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I016280 | chr17 | 16184313 | 16186737 |
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Enhancer Sequence | CACACATCAC CATGCCCAGC TAATTTTTGT ATTTTTAGTA GAGGTGGGAT TTCACCATGT 60 TGGCCAGGAT GGTGTCTAAC TTCTGACCTC AGGTGATCTG CCAGTCTCAG CCTCCCAAAG 120 TGCTGGGATT ACAGGCGTGA GCCACTGTGC CTGGCCAAAA CAATTGTTTT AATTAGCTGG 180 CCGTGGTTGT GCATGCCTGT AGTCCCAGCT ACTCAAGAGG CTGAGGAAGG AGGATTGCCT 240 GATCCTAGGA GGTTGAGGCT GCAGTGAGCT GTGTTTGCAC CACTGCACTC CAGCCTGGAT 300 GACAGAGCAA GACCCTATTT CAAAAAAAAA AAGATATTTC TGAGGAGCCA TGCTCATTCA 360 AGACTCACTG CTCTTAGAAG AGGTGTTAAT CTGGCCAGGT GCCGTGGCTC ACACCTGTAA 420 TCTGAGCACT TTGGGAGGGT GAGGTGGGAG GATCATCTGA GACCTGGAGT TCAAGGTCAG 480 CCTAAGCAAC AGACTGAGAC CCTGTCTCTT AAAAAAAATA AGAGAGAGAT GTTAATCTAT 540 ATTAAACAAT TGAATAGTGT GAAGATTTTG TAAAACTTTT TAAATCACCG ATTATACAAA 600 AGCTCTTATT GAATTATTAA GGAGTTAGCA ATTACTATTA ATGCTGTTGA ATATGAGTAA 660 GAACCCACTT AACTTCAATC AGAATCCATC GATCAAGCTT AAAGCCTTAT CTCATAGTTC 720 CCTTCCTGGT CTGTCAGCAT TGCCTCATAG AGAGGGAAAT ACATCCCGCA TCTGCCTCAT 780 CATGAACTTG GGTGGCCACC AGGATATTGC TCATGAAAGC TGCTTTTCTT TCTTTTTTTT 840 TGTTTTGAGA CGGAGTTTCA CTCTTGTTGC CCAGGTTGGA GTGCAACGGT GCGATCTCGG 900 CTCACTGCAA CCTCCGCTTC CCAGGTTCAA GCGATTCTCC TGCCTCAGCC TCCTGAGTAG 960 CCGGGATTAC AGGCGCCCGC 980
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