| Tag | Content |
|---|
EnhancerAtlas ID | HS139-44847 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr5:137576850-137578480 | 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 | CAGACAAATG ATGAGCCCAG CTCTTGCTAG TTTCAAGTTC CTCCTTTATA ACACGATTTC 60
TATCTCACAG GGTTGTTGTG AGAATTAAAT GAGTAAATGT AAGTAAAATG TTAGCACAGT 120
TCCTGGCACC TAGTATGGAG GCAGCTACAA CTAACTTTCC CCTAGATGGG AAAACCAAGG 180
TTCAGACACA TTAATCTGTG CAAGGAAAAA GCATGGGAAG CTGGGAGATC AGTGTGATCT 240
TGGGCAAGTC ATTTCTCTGA GTCTCAGTTT CCCCACCCTA CCAACTCCCT GGGCTGCTAA 300
GGGGATTCAT TCCTTGGGCA GATATGTACT GAGCACTTGC ATCTTCCAGG CACTTTGGGT 360
GCAGGTACAC AAGGCAGATC CACTAAGTCC CGCTCTTCTG GGGTTTACAG TCTGGACGGG 420
ATAAAGATAC TGTAGAGAAC CTTCTATAGA TCACTTTATA GTGTCACTGT GATAAATGCC 480
ATGAAGTGCT GTGAGGGTGG GTGACACGGT GGTCTGGCCT GGTCTAGGGA GGTCAGGGCG 540
GCTTCCCTGT GACTTCGGCT GGACCTGCAG CATGAGCTGG CTGAGCGTGT TGTACAGCCT 600
GGGCCGAGAG CGCTGGGAAC AGCACCAGGG ACTCTTTGGA ATGTTTAAAC GTTAACCCAG 660
CCGTCGGCAT CGCGCCCCTG GCCTACCCTA AGCCAGGCCG CGATGCTCGC GCCTCCGAGG 720
GCCTCCCGCA GTCAAGCCGG GACCTCGCCC AGCAAGGACT CCAGGGCTGC CCAGGCAGGG 780
GCGCCCGTCC GGCACCGGAC TCCCGCCCTG GGCCCAGCTC CGGCGCTCGG CCAGCCCCGT 840
GCCCCGGGCG GCCGCTGATA GTCGGCTAAT GCGTATCGAA TTTTTGTGGA GTTCGGCCCG 900
CGCAGAGTGC GCGCGGAGGC GCTGCCCGAG CCTCTTAATT CCCTTTGCAT CGATCCTGCC 960
GTTAATGACA TAACCTTCTC CCCTAATTAA CTGACAACTG CATTAGGCGG CGCGCCTCCG 1020
CCGCACGCCG CCCACAGCTT CCCCCACGCA GTTCCGCCCG CGCCGGTGCG GGGCTGGGGC 1080
GCAGCGGCTC CGCCTGGACT CAACTCAGGG TCCGGCTGCC GTGGTGGAGG GGAGAGGATA 1140
GTGTTTCAGG ATCGGGATGC CCCTGCCATC CATATCAGCT CAATAAACAT TTGCCGTTAT 1200
TTATATTGTT GTTGTTTACC TCTTTGCCAC TTAACATACT GTAGCTTACT GTTTCATTAC 1260
AACGACCCAA GAGGCAGAGA GTGGAAATTG GGGCTTGGAG AGGTGGAGGG ACTTCGGCAA 1320
TAACCACGAA TGTGCAGCAA GCTACTGGGG GAGGCGGGAC TCCCACCCTC CTAAGCAGCC 1380
TGGGACTCCA AGTTTGTACT GTTAAGCCCT AGGCTACCCT CCAACGTGTA ATTTAGACCC 1440
TACTAAAGCT ATTACATGCA AAGTGCTTAG CAGAGTACCT GGCAGATAAT GAGCACTCAA 1500
TAAATTTTAG TATGTCAGGC TAATTTACGG AAATACTAAT TTGTGTTTAT TCTCCTTTGC 1560
CTCCCTTTTT CTGGATGGCC AGTTCAGTCA AGTGGCCAGG TTTTCTAATT ACTTGGGCAG 1620
CAGAGAAAGC 1630
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