| Tag | Content |
|---|
EnhancerAtlas ID | HS105-29871 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr16:11632120-11633630 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr16 | 11632604 | 11632654 | | chr16 | 11632717 | 11633030 | | chr16 | 11633071 | 11633139 | | chr16 | 11633256 | 11633606 |
| Enhancer Sequence | TGTATTTTTA GTAGAGATGG GGTTTCACCG TGTTAGCCAG GATGGTCTTA ATCTCCTGAC 60
CTCGTGATCC ACCTGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCG 120
CCTGGCCCGT TTTTTTTTTT TTTTTTTTTT TTTTTTTTAA AGAGACCGAG TCTCACCTTG 180
TTGTCCAGGT TGGTCTTCAA CTTCTGGCCT ACACCAACCC TCCCACCTTG GCCTCCCAAA 240
GTGCTGGATT ACAGGTGTAA GCCACCACGC CCGGCTGAAT TGTACACTTT AAATGGGTGA 300
ATTGTGTGAC ATGTAGATAA CATCTCAATA AAGCTATTGC CAAAGAAGCC AAAAAGTTCT 360
TACCGCAAAG CCCTGTGTGA GTGGCTGTTA TACAGCAGAG TCTACGATGG GGTCTGAAAC 420
CTTCTCCCTG CGTTAGGAGG CCTGCCTCTC CCGGCACTTT TCCCATTTCT TGGCTACTCA 480
GAGATGCACC AGCCACTTCA CCTGTGGCTC AGCTCTATAA TCGACCCCTG CTTCCAATCC 540
CCACGTCCTC CAAGCAGAAA TACGCCTGCC CAGGATCACA GGTACCCTAG CTGCTAAGGC 600
CTCCGTGGTA ATGAGCCCTT ATGTAAAGAC GACAGCCCCG TGCCCAGTCC CCTTCCTGCC 660
CTTGCTTCCA GGGAATGGGC CCTATTAGCC ATGCCCTGAG CAGGACACAC GTGCAGCCCT 720
AGATCTGTAG ACGCAAGACT CACTCCAAAG ATGGGATTCT CAGCTCAGGG AGGGAGGGAG 780
GCAGCCCCCA GGGCCCACCG GTGGAAGGAA TGTGGGGGCC TTCGAATGAC CTGCAAAGGT 840
GGCTCCTGGC CCCATCCTCA CCTGAGCCAG ATGTGTGAAT ACAGACGCCC GCCCCTGGCA 900
GCAGACAGTG GGAAGGAGAC ACAGGGGGCT GATTCTTGCA AAGTTGAGTG TCATTTCTTG 960
GCTTGCTCTG CTCCTGCGTA TCAAAGCTGA CCACAGCCTG GTGCTCATTG AGACCTGTGT 1020
CTCAAGGGTT TCCTAGTTTA CCGAAGAGCT GGCTCCGGTG GGCTGTAGGG CAAACGCACC 1080
TGAACGCAAT AACCTGCGCA CATCCTTAGG ATGACCTGGA TGGCAGACTC ACCTGAATGT 1140
GAGTCCCAGC TACGGAATCC GGGAATGGCC AACCTGGAGA TTTGTTTCCT GTCTATGAGA 1200
AACATCTGAG CCCCTGGCCC ATCCCATGAA ACACAGGCCC TCCAAGGGAT GGAGGCTCTG 1260
AGTTTTAGGT TACATGAAGG TTGCCAGGTG GAGGTCGTTA AGGGGAGGGT GTTAAGTGAA 1320
AATGCTGAAT AAACTGCATG CTGTTTGCAA GTGGCTGCAG TTTCCCTCTC CAGCCCACCA 1380
GCACCTGCAC TCTCTCCCCT GTGTCTAAGT CCCGAATCAA ACCCAATGTC TCCTTTGCTG 1440
GCTCTGCATT TCTTCTTCAG CCTCTTGAAC TTGTTACCTC CCTAGTGAAA CTAACAGGGT 1500
TTCAGCACAA 1510
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