Tag | Content |
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EnhancerAtlas ID | HS098-44312 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:17145670-17146650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr5:17145815-17145830 | TGAACTTCTGACCTC | - | 6.38 | RARA | MA0729.1 | chr5:17145812-17145830 | TCTTGAACTTCTGACCTC | - | 6.88 |
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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 |
GH05I017145 | chr5 | 17145774 | 17146765 |
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Enhancer Sequence | CACTGCAACC TCCGCCTCCC GGGTTCAAGT GATTCTCCTG TCTCAGCCTC TGAGTAGCTG 60 GGATTACAGG CGCCTGCCAC CATGCCCAGC TAATTTTTGT ATTTTTAGTC GAGAGGGGAT 120 TCCACCACGT TGGCCTGGCT GGTCTTGAAC TTCTGACCTC AAGTGATCGG CCTGCCTTGG 180 CCTCCCAAAG TGCTGGGATT ACAGGTGTGA GTCACTGCAT CTGCCATGTT GCCGTTTTCA 240 AGGGAACTAA GCAAAATCTT ACAGCAAATT AGGGATAGAA TCAATAAAAT CACCTGTTTA 300 ATGTAAAGTG TTGGATTAGC AAACTGATTT TTGAGGTGCT TGGTTTTCCT TATTTTTGTT 360 GTTTAGGTAA GTGTTCTTCT AATCTGTATT TGAAGTTGTC TTTCTCTTTT GATTGTATGC 420 CTTGTGGCTA ATGACTCATT ACTGCACCTG ACATCCAGGG AATTCAGTGG CTTTGTAAGC 480 ACCCCCTGGG AGGAAGATTA CTTGGACAAA CAGCAATGAA AACAGTTCGA CTTACACATC 540 TGAATGAAAA TAAAATGAGA ATTGTTTTCA TTCTATGTGT TTTTGTACCC TTTTGGTGAA 600 TGGCTACTTC CCCAGTGCTC CTAGTAAATG CAAAGTACTG CTCATTCAGA GTAGTGAGCA 660 CCCATTGTTG GCCTCAGTGT TAATTTCTCA CAGCCTGGAG AGGTTATAAT AAGCAGATGA 720 TGGAATGCTT ATACTAGGGT CTGTGTTGTT ACTATTGACC TTGCTGTACA TGTTCTCTAA 780 CGTACATTTC CCCCAAATTC ATCAAGTGGG ACAATATCTT CTTCTCTTAA GGAAAAAGCC 840 CTATGAGGAC GGAGCCAAAG GTCTCTCCTC ACTAGGACCA ATGCAGACTG CAGATCTGCG 900 AGACAATCCG CTGTAGTCAC AGCATCTTCT GTATGTGAAG CCTTTGAGAA ACAAAGGTGA 960 CTTGAGGAGG TTGACTTTTG 980
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