Tag | Content |
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EnhancerAtlas ID | HS053-12569 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr14:73427900-73429420 | 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 | CCCTCACACT AACCCCACGG CACAGTTTGG GAAACAAGTT TGTTGAGTTA AAGTGGTTTG 60 GCAAGAAGGG CTGAGCTGGG ATTAAGATTC CGCTCTTCCC AACTCTGAAG CCCCTGTTCC 120 CCTCACTGCT GTGTCCTGCT CATTTTCCAG GCCCAGGTTA ACAACAATGG GAAAGAGTTG 180 AGAGATACTT TTCTAACAGG GTAAACCCTC CTCCCAGCCC AACTCCACCA TCCTGGGCCA 240 CTCCTCTACT CACATGATCC TTTGTACCAT TTGGTCCAAT TGATCTTGAT CTCATCCATT 300 TTTTCCACAT GGGTCAGAGA CAAGGGTGAG ATTTTTCTCA TTTCTCGTGG GAGAAAGGCA 360 AGCTCTGCCA AGCCCAGAAT TTCTGGCCCC TCCTGTCCCA GCACAAACCA TTCACAGTCT 420 TCCCGCAATT ATTCCTGGTG CAGGGTTTTA TTTCTAGGAA GCCTTCTGTC CCTCAACCTC 480 ACCAGCCCTT GGCTTTTCAG CCCAGAGGCT CAGGACATTT GAGGATTGCG TGTTTGGCTG 540 TGGGCATGGG GAATGCAGTG ACTACACCTG GTTGGCATCC CATACCACAC CCAGGGGAAT 600 GGGGAAGCCA AGAGGTGGAC TGGAAGCAGG CTCAGGCCTC TCTCTCCTTG CCCCCAAGGG 660 CATCCTCTCC AGCAGATGGC CACTACAATG CTGATGTCAA ACTGGTCAGT GGGTTCAGTG 720 GAAGGTTTGG CTACCGCGGG AACACCCCAG CTCTCCGTCG GAGCACGTCT GTCTTTGGAG 780 AGGTCACCCA CTTCCCTCTG TTCTAACAGC ATCTCTTCCC TTCATAGCCC TCAACCTGAA 840 TTTCTAAGAC AGATGTTTAG GTGAACTCTC AATGTTATTT TACATTAAAA AAATTTGTGT 900 CTCCAAGTGT GCCGTTTCTT CCCTGAGACT GGAGGAAGGA GCCAGCTGTA CTCTCAGCTT 960 CTCTTACCCT GGAGAGGAGG TGAGACGAGA AGGGCTTCTC AGGCCTATGC CCTTGCACTC 1020 GGAGAGGCTT CACTTCTACC CTGCCAGTGG GATAAGAAGG AGCCACACTA TTCATCCTCA 1080 ATAAAACACT TCCCCAGCTA TCAGCAGGAC CCCAGGATCA GAGCTGGCTA CTGTTTCCAT 1140 CAAGAACAGA GCAAAGGCCA AGCTCCGTGG TTTATGCGTG TAATCCCAGC ACTTTGGGAG 1200 GCCGAAGTGA TGCCGAGACA GGAGGATTGC TTGAGCTTAG GCAGTTGGAT CACTTGAAAC 1260 CAGCCTGGGC AACATGCCAA AACCCTGTCT TTACAAAACA CACACACACA CACACACACG 1320 CATGCACACT CTCTCTCTTA GCCCAGGCTG GAGTACAGTG GTGTGATCTC AGCTCACTGC 1380 AACCTCCGCC TCTCAGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCTAG TAGCTGGGAT 1440 TACAGGCGCC TGCCACCACG CCCAGCTAAT TTTTTTTGTA TTTTTAGCAA AGACGGGATT 1500 TCGCCATGTT GGTCAGGCTG 1520
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