Tag | Content |
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EnhancerAtlas ID | HS092-36419 | Organism | Homo sapiens | Tissue/cell | HFF | Coordinate | chr8:21541040-21542480 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | 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 |
GH08I021683 | chr8 | 21541041 | 21542695 |
| Enhancer Sequence | GGACCATTTC CAGTTGTGAA GAAGATCAAG TTTCCTCCAT TTGAAAGAAA AGGTTATTCC 60 AGCAGCCCCC ATCACCACCA CGCACTCCAG GTAGAAATAC CAGAAATACA TTTCCCAGAA 120 TAAGATATTT TAGTACAGAT CCCTCATGTC ACTGCAGCCT CCCACTCAGC CAGCTTTCTA 180 GCAAAACGAG AATTAAGAGT AATTTCAGGT TGCTGGGGCC CCTGAAAAAG GCTTATCTTC 240 CACTGAGGAT AAAAGTGAAG GATAGACTGG GCCAGGCGGG GTCATTCCAC AAGGATTTGT 300 TTGACCAACC AGGCTGGACC CTGACTATTA AATGGAGTAG GATGAGAGCA GCGACCTCAT 360 CTTACATTGT GAGCCTCCTG TGTGTTGGTG GGCAGGGAAG GAGAGGGGCG GGGTCAGTCC 420 ACTGTGCTGG GCTGGAAAAA ATCAAAGAGT TTTTCCTGGA AGACTCTCTT CTGGCTGTAA 480 GAGCTTCAAC ACACGCAGTC ACGCTCACCA CGGTGGTTGT GCAAACCTCC CACAGAGATG 540 TTTGATGAGA TTAGTCACTT TCTGCCAGGG TGGTTGGTCC ATGCGTAGGA GACTTCATGA 600 CCTCTGATGC TGGGCAGTGT CTAGGTCAAG GTGGTGACTC AAGTGTGCCC TCCTCCAGGG 660 AGGGAGGCCA GGCGGGGGCT GAGTCATTGC TTCACATGGC CCCAGAGGTT GGCTTCCCAA 720 GAAATGCTGT CTTGAAGGAG TGGGAACAGG CCAGCGTGTA AGGTGCCACG CACAGAGCAA 780 GCTCTAAGGT GGCAGTCCAC AGCTCTGGAC TAGAGGCTCA GAGAAAAATT GAAGCAACCA 840 AGCATGTGGC GGTGTTTGCT GAAAGGGAGA TGAATTCTGC CTCCTTTCAA GTCATTTTTC 900 CCCAGGCCGG TGAGTTCAGG AATGGCTGCC AGTCACAGAA TCACAGAATC CCATTGCCGA 960 GGGAAGGTTG GGGAGCAGCC CCTCTGACCT CTCCCTCTGA AGATGAGGGC AGGAGAGTCC 1020 AGGGAGGGTA AGTGACTTGC CCACAGCCAT GCAGCGCTCT CAGGGGCTTC TCTGTGCACT 1080 CAGGACCCTT GTCCCCTCCC CAGCCACTGG GGTGGCAGCT CCATTTGCTC TTGGCCACAA 1140 GTTCTCCGCA AGCACACAGA GAAACCTTGG TGCAAATTAG AGAATGATGC CCCCTCCTCG 1200 GGGCTGAGGC CCAGGTTGGG TGCACAGATG GGTGAGTTGA GGGTGGCTGG CTTTCAGCCC 1260 CATTCGCCCT GCTTACCAGA TGCCCCTGAT CAGAGTACAA TCTCACAGTG GCAAGCAAAG 1320 TCCCCACATT CCAGCCCACA CCTATGTGTG CCTGGTCCAC AGGCTACCTG CCTTCTCTCC 1380 TTGCACCTCT GGACCGCATG CAGGACGGTT CCTCCCAGCT TTCTCCTCCA CCAACTCCCA 1440
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