Tag | Content |
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EnhancerAtlas ID | HS184-21951 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr3:184088930-184089720 | 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 |
GH03I184371 | chr3 | 184089189 | 184089788 |
| Enhancer Sequence | CCACTGATAA CTCACCTGGC TTCTCTGAGC CTCAGTTTCC TCATCTCTAA AACAGAAAAG 60 ATAATACCTA CCTTACAGAG TTGTGTGAAT GTTACAAAAG GTAAAGTACA CGAGGTTCCT 120 AGCACATTGC CTTTCATTCT GCTGCTTTGG AATGCCTTTG GTGACCCTGG GGTATTTGTG 180 GCAGTGTTTG GGTTTCTGGG TTCCTGGCTC CTCTACCTCC GTGGTAGCCT TTCCTTCCTC 240 AGGGGTCGGG GAGAGGAAGA AGCTTCCACT AGTTTTCCTA CAGGAACCTC TGGAGGTAGC 300 AGGTTGATTT TTGCAGTGGA ATTTGTGTTT TTGTGCAACA CAAACCTTTT CCTGAGCACC 360 AAGGCAGCAC TTATTTGCAA AGCCCCATAA GCCTGACTCC TTTTTAGAGA TCCCCTAGCA 420 GAGTTTATGG TGGTCACACA GAGCTGCTTT TTAGATGCAT TTGCGGGAAC TGGGAAATGA 480 GCCTTCAACT TGTACTTGAC TTGTACTTGT TCTCCTGCTG TGTGAGCTCA AGGAGCCTGA 540 CTCATGCCAC TTCCTGCACT TCCTCCTGAC CTCCACAGGA GGGAGGCAGG CGTCCATGCC 600 TGGCAAAGCC TCCTGCTGAG CTGCCAAAGC TCTAGCTGTT TGCTCAGCTG TCACATCCAG 660 GTCCTGTCTT TACTGAACTG TCTACACAGC CTTACCTGGG GTGTGAGGCT CTCCAAGGCT 720 TCCTGTTAGC TTTTTTGTTT GGGGTGGCAG GGTGAGGGGG ATCTATTGCC ACCCTCGAAG 780 AACATCTTTC 790
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