| Tag | Content |
|---|
EnhancerAtlas ID | HS095-24747 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr5:137576600-137578440 | 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 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I138241 | chr5 | 137577221 | 137578130 |
| Enhancer Sequence | CATCCCTAGT GTGGGGCCAG ATGAAGGAGA TGGAGCCAGA AGCTGCCAAG GCTGTGGGTC 60
TCCTAGCTTC TCCTGTCCTC CCACCCTCAG TCTGTGCCTG TGGCTCCCGT TGTCCAAACC 120
CAGCCAAAAG CCAGCTGACA AGGGAGCCTG GGAAATGCAG CCTGCCTGGG GATGGGATGG 180
GGATGGAGTG TAGGGGTAGC CCACATGTGA CACAGAGTAT TAGAAGGAGA GCAATGGATC 240
TGAAGGCAAA CAGACAAATG ATGAGCCCAG CTCTTGCTAG TTTCAAGTTC CTCCTTTATA 300
ACACGATTTC TATCTCACAG GGTTGTTGTG AGAATTAAAT GAGTAAATGT AAGTAAAATG 360
TTAGCACAGT TCCTGGCACC TAGTATGGAG GCAGCTACAA CTAACTTTCC CCTAGATGGG 420
AAAACCAAGG TTCAGACACA TTAATCTGTG CAAGGAAAAA GCATGGGAAG CTGGGAGATC 480
AGTGTGATCT TGGGCAAGTC ATTTCTCTGA GTCTCAGTTT CCCCACCCTA CCAACTCCCT 540
GGGCTGCTAA GGGGATTCAT TCCTTGGGCA GATATGTACT GAGCACTTGC ATCTTCCAGG 600
CACTTTGGGT GCAGGTACAC AAGGCAGATC CACTAAGTCC CGCTCTTCTG GGGTTTACAG 660
TCTGGACGGG ATAAAGATAC TGTAGAGAAC CTTCTATAGA TCACTTTATA GTGTCACTGT 720
GATAAATGCC ATGAAGTGCT GTGAGGGTGG GTGACACGGT GGTCTGGCCT GGTCTAGGGA 780
GGTCAGGGCG GCTTCCCTGT GACTTCGGCT GGACCTGCAG CATGAGCTGG CTGAGCGTGT 840
TGTACAGCCT GGGCCGAGAG CGCTGGGAAC AGCACCAGGG ACTCTTTGGA ATGTTTAAAC 900
GTTAACCCAG CCGTCGGCAT CGCGCCCCTG GCCTACCCTA AGCCAGGCCG CGATGCTCGC 960
GCCTCCGAGG GCCTCCCGCA GTCAAGCCGG GACCTCGCCC AGCAAGGACT CCAGGGCTGC 1020
CCAGGCAGGG GCGCCCGTCC GGCACCGGAC TCCCGCCCTG GGCCCAGCTC CGGCGCTCGG 1080
CCAGCCCCGT GCCCCGGGCG GCCGCTGATA GTCGGCTAAT GCGTATCGAA TTTTTGTGGA 1140
GTTCGGCCCG CGCAGAGTGC GCGCGGAGGC GCTGCCCGAG CCTCTTAATT CCCTTTGCAT 1200
CGATCCTGCC GTTAATGACA TAACCTTCTC CCCTAATTAA CTGACAACTG CATTAGGCGG 1260
CGCGCCTCCG CCGCACGCCG CCCACAGCTT CCCCCACGCA GTTCCGCCCG CGCCGGTGCG 1320
GGGCTGGGGC GCAGCGGCTC CGCCTGGACT CAACTCAGGG TCCGGCTGCC GTGGTGGAGG 1380
GGAGAGGATA GTGTTTCAGG ATCGGGATGC CCCTGCCATC CATATCAGCT CAATAAACAT 1440
TTGCCGTTAT TTATATTGTT GTTGTTTACC TCTTTGCCAC TTAACATACT GTAGCTTACT 1500
GTTTCATTAC AACGACCCAA GAGGCAGAGA GTGGAAATTG GGGCTTGGAG AGGTGGAGGG 1560
ACTTCGGCAA TAACCACGAA TGTGCAGCAA GCTACTGGGG GAGGCGGGAC TCCCACCCTC 1620
CTAAGCAGCC TGGGACTCCA AGTTTGTACT GTTAAGCCCT AGGCTACCCT CCAACGTGTA 1680
ATTTAGACCC TACTAAAGCT ATTACATGCA AAGTGCTTAG CAGAGTACCT GGCAGATAAT 1740
GAGCACTCAA TAAATTTTAG TATGTCAGGC TAATTTACGG AAATACTAAT TTGTGTTTAT 1800
TCTCCTTTGC CTCCCTTTTT CTGGATGGCC AGTTCAGTCA 1840
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