Tag | Content |
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EnhancerAtlas ID | HS062-14100 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr6:44138940-44140030 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 44139822 | 44140020 | chr6 | 44139913 | 44140005 |
| | Number: 1 | ID | Chromosome | Start | End |
GH06I044172 | chr6 | 44140025 | 44141137 |
| Enhancer Sequence | GGATGCACAG CACCCTGCCC CTGGACCCCA CCCAGCAAGG GCTGAGATGC CTAGGAGACA 60 GGTGGCAATG GAGGTCTGTA GTGCTCATCT CCCATAGGAT TCCCTTTAGC CGAACTTCAG 120 GCCAGGGACA CTGCCTCATA CCCACTTCAA TGCCTAGCTC CAGGGACCCT GCTGGGGCAC 180 ATACTGAGCC CTGGGTCCCC AATATAATGT GGGTGACATG AGGGAGAGAC CTCTTGGGAA 240 CTTCGTGGCC ACACCAGTGT ACTCACAGGG TGCAGGAAGG TGACTGGATC TGTTGGAAGA 300 ATGTGGAGAG TATTGGCTCT GTCTCAAAGA AAGCAGGTTA CTGGTCAGGT GCAGTGGCTC 360 ATACCTGTAA TCCTAGCACC TTGGGAGGCC AAGGCAGGAG GACTGCTTGA GCTCAGGAGT 420 TCAAGACCAG CCTAGGCAGC ATAGTGAGAC TCTGTCTCTA CTTATATATA AAAATTTACT 480 TTAAAAAAAA ATAGGTTCCT AGAGCCTGAG GCCAAAAGTA CCTCTTTTCC AAACTCAAGA 540 AAAACAAAAG GATGTGTCTC TCACATAATA GAAAAGGTAC AGCCAGGCAC TGTGGCTCAC 600 ACCTGTAATC CCAACACTTT GGGAGGCCAA GGCTGGCAGA TCTCTTGAGG CCAGGAGTTT 660 AAGACCAGCG TGGCCAACAT GGTGAAACCC CATCTCTACT AAATATGCAA AAATTAGCCA 720 GGTGGGGTGG CGGGCGCCTG TGGTCCCAGC TACTCAGGAG GCTGAGACAG GAGAATCGCT 780 CGAACCCAGG AGGCAGAGGT TGCGGTGAGC TGAGATCATG CTATTGCACT CCAGCCTGGG 840 TGACACAGCA AGACACTGAC TCAAAAAAGA AAATGTACAG AAACTCACCT TACTAGAGTC 900 TCTCCGCCTT CAGTTTCTCC CTGTTTACCT CCTTCCTGAA CACTCTTTAG TGGGAGGGCT 960 GAGGGAGGGT GCCTCTCCGC CGGGGGGGTG AGAATGGGGT ACAGGGTCAA GTTCCTGCTC 1020 CCCTAGGCCT TGGATTCTGA GGCCCACCCA CACATATGGG GTTGCTCAGG GGTGGCAAAG 1080 CCCTGCCTGT 1090
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