Tag | Content |
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EnhancerAtlas ID | HS139-16981 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr14:73427830-73429340 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 73428111 | 73428893 | chr14 | 73428898 | 73429305 |
| | Number: 1 | ID | Chromosome | Start | End |
GH14I072960 | chr14 | 73427662 | 73430109 |
| Enhancer Sequence | GTGATCCTCT GGCCTCAGCC TCCCAAAGTG CTGGCATTAC AGACACGAGC CATTTGTAAG 60 ACACTTCTCA CCCTCACACT AACCCCACGG CACAGTTTGG GAAACAAGTT TGTTGAGTTA 120 AAGTGGTTTG GCAAGAAGGG CTGAGCTGGG ATTAAGATTC CGCTCTTCCC AACTCTGAAG 180 CCCCTGTTCC CCTCACTGCT GTGTCCTGCT CATTTTCCAG GCCCAGGTTA ACAACAATGG 240 GAAAGAGTTG AGAGATACTT TTCTAACAGG GTAAACCCTC CTCCCAGCCC AACTCCACCA 300 TCCTGGGCCA CTCCTCTACT CACATGATCC TTTGTACCAT TTGGTCCAAT TGATCTTGAT 360 CTCATCCATT TTTTCCACAT GGGTCAGAGA CAAGGGTGAG ATTTTTCTCA TTTCTCGTGG 420 GAGAAAGGCA AGCTCTGCCA AGCCCAGAAT TTCTGGCCCC TCCTGTCCCA GCACAAACCA 480 TTCACAGTCT TCCCGCAATT ATTCCTGGTG CAGGGTTTTA TTTCTAGGAA GCCTTCTGTC 540 CCTCAACCTC ACCAGCCCTT GGCTTTTCAG CCCAGAGGCT CAGGACATTT GAGGATTGCG 600 TGTTTGGCTG TGGGCATGGG GAATGCAGTG ACTACACCTG GTTGGCATCC CATACCACAC 660 CCAGGGGAAT GGGGAAGCCA AGAGGTGGAC TGGAAGCAGG CTCAGGCCTC TCTCTCCTTG 720 CCCCCAAGGG CATCCTCTCC AGCAGATGGC CACTACAATG CTGATGTCAA ACTGGTCAGT 780 GGGTTCAGTG GAAGGTTTGG CTACCGCGGG AACACCCCAG CTCTCCGTCG GAGCACGTCT 840 GTCTTTGGAG AGGTCACCCA CTTCCCTCTG TTCTAACAGC ATCTCTTCCC TTCATAGCCC 900 TCAACCTGAA TTTCTAAGAC AGATGTTTAG GTGAACTCTC AATGTTATTT TACATTAAAA 960 AAATTTGTGT CTCCAAGTGT GCCGTTTCTT CCCTGAGACT GGAGGAAGGA GCCAGCTGTA 1020 CTCTCAGCTT CTCTTACCCT GGAGAGGAGG TGAGACGAGA AGGGCTTCTC AGGCCTATGC 1080 CCTTGCACTC GGAGAGGCTT CACTTCTACC CTGCCAGTGG GATAAGAAGG AGCCACACTA 1140 TTCATCCTCA ATAAAACACT TCCCCAGCTA TCAGCAGGAC CCCAGGATCA GAGCTGGCTA 1200 CTGTTTCCAT CAAGAACAGA GCAAAGGCCA AGCTCCGTGG TTTATGCGTG TAATCCCAGC 1260 ACTTTGGGAG GCCGAAGTGA TGCCGAGACA GGAGGATTGC TTGAGCTTAG GCAGTTGGAT 1320 CACTTGAAAC CAGCCTGGGC AACATGCCAA AACCCTGTCT TTACAAAACA CACACACACA 1380 CACACACACG CATGCACACT CTCTCTCTTA GCCCAGGCTG GAGTACAGTG GTGTGATCTC 1440 AGCTCACTGC AACCTCCGCC TCTCAGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCTAG 1500 TAGCTGGGAT 1510
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