Tag | Content |
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EnhancerAtlas ID | HS113-11510 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr14:73427870-73429480 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I072960 | chr14 | 73427662 | 73430109 |
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Enhancer Sequence | AGACACGAGC CATTTGTAAG ACACTTCTCA CCCTCACACT AACCCCACGG CACAGTTTGG 60 GAAACAAGTT TGTTGAGTTA AAGTGGTTTG GCAAGAAGGG CTGAGCTGGG ATTAAGATTC 120 CGCTCTTCCC AACTCTGAAG CCCCTGTTCC CCTCACTGCT GTGTCCTGCT CATTTTCCAG 180 GCCCAGGTTA ACAACAATGG GAAAGAGTTG AGAGATACTT TTCTAACAGG GTAAACCCTC 240 CTCCCAGCCC AACTCCACCA TCCTGGGCCA CTCCTCTACT CACATGATCC TTTGTACCAT 300 TTGGTCCAAT TGATCTTGAT CTCATCCATT TTTTCCACAT GGGTCAGAGA CAAGGGTGAG 360 ATTTTTCTCA TTTCTCGTGG GAGAAAGGCA AGCTCTGCCA AGCCCAGAAT TTCTGGCCCC 420 TCCTGTCCCA GCACAAACCA TTCACAGTCT TCCCGCAATT ATTCCTGGTG CAGGGTTTTA 480 TTTCTAGGAA GCCTTCTGTC CCTCAACCTC ACCAGCCCTT GGCTTTTCAG CCCAGAGGCT 540 CAGGACATTT GAGGATTGCG TGTTTGGCTG TGGGCATGGG GAATGCAGTG ACTACACCTG 600 GTTGGCATCC CATACCACAC CCAGGGGAAT GGGGAAGCCA AGAGGTGGAC TGGAAGCAGG 660 CTCAGGCCTC TCTCTCCTTG CCCCCAAGGG CATCCTCTCC AGCAGATGGC CACTACAATG 720 CTGATGTCAA ACTGGTCAGT GGGTTCAGTG GAAGGTTTGG CTACCGCGGG AACACCCCAG 780 CTCTCCGTCG GAGCACGTCT GTCTTTGGAG AGGTCACCCA CTTCCCTCTG TTCTAACAGC 840 ATCTCTTCCC TTCATAGCCC TCAACCTGAA TTTCTAAGAC AGATGTTTAG GTGAACTCTC 900 AATGTTATTT TACATTAAAA AAATTTGTGT CTCCAAGTGT GCCGTTTCTT CCCTGAGACT 960 GGAGGAAGGA GCCAGCTGTA CTCTCAGCTT CTCTTACCCT GGAGAGGAGG TGAGACGAGA 1020 AGGGCTTCTC AGGCCTATGC CCTTGCACTC GGAGAGGCTT CACTTCTACC CTGCCAGTGG 1080 GATAAGAAGG AGCCACACTA TTCATCCTCA ATAAAACACT TCCCCAGCTA TCAGCAGGAC 1140 CCCAGGATCA GAGCTGGCTA CTGTTTCCAT CAAGAACAGA GCAAAGGCCA AGCTCCGTGG 1200 TTTATGCGTG TAATCCCAGC ACTTTGGGAG GCCGAAGTGA TGCCGAGACA GGAGGATTGC 1260 TTGAGCTTAG GCAGTTGGAT CACTTGAAAC CAGCCTGGGC AACATGCCAA AACCCTGTCT 1320 TTACAAAACA CACACACACA CACACACACG CATGCACACT CTCTCTCTTA GCCCAGGCTG 1380 GAGTACAGTG GTGTGATCTC AGCTCACTGC AACCTCCGCC TCTCAGGGTT CAAGCAATTC 1440 TCCTGCCTCA GCCTCCCTAG TAGCTGGGAT TACAGGCGCC TGCCACCACG CCCAGCTAAT 1500 TTTTTTTGTA TTTTTAGCAA AGACGGGATT TCGCCATGTT GGTCAGGCTG GTCTCAAACT 1560 CCTGACCTCA CCTTGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA 1610
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