Tag | Content |
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EnhancerAtlas ID | HS053-19219 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr19:13802130-13803590 | SNPs | Number: 2 | 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 |
GH19I013692 | chr19 | 13802921 | 13803010 |
| Enhancer Sequence | ATTTTTTCAT GTATTTTTGT AGAGATGGTC TCACTATGTT GCCTAGGCTG GTCTCAAACT 60 CCTGGGCTCA AGCAATCCTT CCACCTCAGC CTCCCAAAGC ACTGGGATTA CATATGCCAG 120 CCACCGCACC TTGGTCTGCT GCCTCTTTTT ATAAGGATGC TAATCCTATT GGATCAGGGC 180 CCCACCCTGA ATACTTCATT TAACTTAATT GCCTCCTAAA AGTCTTATCT CTGAATACAG 240 TCACATTGTG GGGCACAGGG ATTTGGAGGG CACACAAACA TTTAGTCCAT AACTGACCCC 300 TAAACCTATT GATGATTGGC TGCCAGGGAA GGTTGAGCAA GGTAGGCTCC AAGGCACTCT 360 GGCCCTCCAT ATGGGCAGGG CAGCTCCAGG GCCCAAGAAC AACCTCTGAA GGTCACAGGT 420 GTGAGCAGGT AGCATGTAAG CATTAAGAAA CCAGGGGATG GATGCACTGA GGTGGGGTGA 480 GGTCCGGGTG TGGCTGCCCA CACTGCCTGC TACTCTGATG CTGTATCAGC AAGAAACAGC 540 TTATACATTT CTGTTGTAAT GGGGGAAGCA AACTTTAATC ATACATCTGC AGATTTCTCT 600 CACTCTACGC CAGCCTGCAG ATGTCTTCTG CTAGAGTTAA AAATTTCCAC GGAATTATCT 660 CCAATCTCCT CTCACAGCCT GGTAATTTGG CCAAAAGAAA TCCCAGATGT TTCAAAGAAT 720 CCCTAATAGT GACTGTAGGG CTTTGATTTC TCCTCATCCA GTTGGTCCCA GGGCACTGCC 780 AAGCCCTGGT TGGTGTCCTT GTCAAATTGC TCCGAGAGTG AGCAAAAAAA CGGAGAAACT 840 TGTGCCCAAA ACCCAATCAA GCATTTGTCT TAAAAGCACA CTCGCCTTGA AAGCCAGCCA 900 ACTTCTGTGA AATAGAAAAG AATCCATTTT CTGCTTCTAT TTCTTGGCCC TTGAACAGGC 960 AGTGACTCAA GACTCAAGTC AGTGGTTGGT GCAGCTGCAA TGAGACATCC GTCAGTGAGC 1020 TGGCATCTCT GACAATGGCG TGTGCCCACA GAGAGGCTGT GACTCAGGAG GGCAGGTGGC 1080 ACTCCATGAT CCCCCAAAGC AGCCAAGCCA GGTGGGGTGC CAAGCATCCC AGGTGCTCCT 1140 GAGCTGGAAG ACCGACAGTT TTCTACCAGT TGAAGTCGTG TTTGGCAAAG AAACCGTTCA 1200 GCCCTTTAAC AGATATTGAC AGCCTGCTAG TTTCCAAAAT GGGGTCAAAA GATGGAGATT 1260 CTCCTTTGAT GGTGTCAGCG GGTGCATAAT GGATGTGTGG ATGTTCTTTG TGCTCAGAAA 1320 CGTCTGCCGT TCCATCCAGT TGCATGCTGA AGGGAGGTGG GGAGCTGCCA ACTCCTCCAC 1380 GACCCATTTC AAAGTATTAA AAGAATTGTT AGCAATTCCA GGTTGCTGGT GAAAACATCT 1440 CCTTGGTTTT CTTTCCCCCA 1460
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