Tag | Content |
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EnhancerAtlas ID | HS112-12489 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr6:29780320-29781730 | 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 |
| Enhancer Sequence | CAGATCGCCT GGCTGCAGAG TCTAGTTGCC CTCAGTGGAG CCAGCGAACC CAGGAGCTGA 60 CACCAGAGAC TGAGATCTCA GCTGTGCACT GCCCTGGTGG TCTCCTGTCC CAACCAGGTG 120 TTGACCCAGG CCTTGCAGGC TCACGCGCTC TGGAAAAAAG AGAGAAACCA ATAAATGCTC 180 CCCTGGGTGC AGAGTGCTGC TTTTTATTCC CTGAGGAGTT CTCCCTCCTC AGTCACTCCC 240 AAATCAGATT TACCCTTTCT CTGACGGAAG ATGACGTCCC CACTTTTTTC TCCCTCCCAT 300 CGCACTTTTC CAGCCCCTGC CAGTCCCCTC CCGTGACTCC ATCAACATCA GCACCTGCCC 360 TGTGTCCACC ATCCATTGTG CAGTGAGTGA AAGGACCCAG GACTAAGGAA CAAGACCCAG 420 GAGGAAACTC AGTGCCCTTT CCTCCTCCTC TCAAGCCTGA CCAGCCCTGA CACAGTGAGA 480 GGCCTCCCCA AAGAGAGGCC CTGGCCCTGT CTCCATGTCC TTCCAGGTCT GGGCCAAGTC 540 ACACACAGTC CTTCTCTTCC TGAGACCCCA GGCCCTCTTC ACCTGCAGAG GCACCTGCAT 600 ACCAGGGCAG GCCCTGCACG CTGTGGGTTC TGCCCTCCAC CAGCAGCTCA CTGTTCCTCC 660 CCTCCCAGCT CTGAGCAGAC AGCTCCTAAC TAGAGATCCT ATCAGGAAGC CCTGGGGCTC 720 ACAGGCCCTG CATGGAAATA TGTGGCTGCC ATGGAGTCTG CACCTGACCT GATGCTGGGG 780 ACCCCCTTGC TCAAGGAGGC CCAGCCTGCC CTCCCCATAA CCTGCATTTG GGCTGTGCTT 840 GCTCCTGCCT GTCCACTCAA CCCTGGAAAT GCAGCTCCAC CCCAGGGCTG CTGCTTGGTG 900 AGGCTGCAAG CCCTTCCTGT CCCATTCCTA ACAGGGATTC CACCCAGGCC ACTGCCATCG 960 CAGCTCACAG GGGATCTTCT TCGCCTGTGG AGTAGGGGGT TTCTTCAGAC CCCTCATCCT 1020 GAGGCTGCCT CTACGCACCC TCTGCACCTG GGGATTGCCA CTGCCACAGG CACTGTCTCC 1080 CACATGGACC CTCTGAGAAA CGAAGCCCCA AATTTGACTT CCTGTTCTAT TCAACATCCT 1140 TTACAACATC AGTATTGGGG GAAATCCTAT TAAGATTATC CAGCTGAAAT TATGTTGATG 1200 GACACCAATA CTTAAAGCAG GAATTTTGAG AAACTAACAT GTAATTTTCA TGCCTTTTTC 1260 TGGCCAATGT CCCAGTGACC TACGAGAAAA CCTTTCCTGC CTACAGGGAA CCAGAACTGA 1320 CAATCCCTCT ATAGGAGACA CCGCAGGTGA GAGCAGGAGC AACCACAGAC CTGCACTGCC 1380 CGTGCTGTGG TTGCCTCCTG GACGGGGCCC 1410
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