| Tag | Content |
|---|
EnhancerAtlas ID | HS175-17965 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr21:45001280-45002670 | | | 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 |
| GH21I043581 | chr21 | 45001401 | 45002360 |
| Enhancer Sequence | AAAGAAAAGA AAGAAGGATA AAAGGAGTCA CTTATGAAAG ATGCTGGGAT AACTCAAAAT 60
CTGAGGAAAA GCTATACAGC CCACCTGGAC AGGGATAAAG CTGACTGCAA GCCATAGGGC 120
TCCTCTGCAT CTCAGGTCAG CATTTATGTC TTGGCTTCAG CAACTGACAA CACAGATAAA 180
TTTTCTCCAG GTGGCCAGGA ACACGGCCAC AGGCAGCTCT AGAGTCACAT CCAATAGTTT 240
CACGGCCCAA GAAAGGCAAA AAAAACACTG TTCTTCAGCA GCTGAAGCCA GAAAACTCCT 300
GGAGAAAGAC TATGGCCCAG CTCAGAGCAC ACACCCACCA CTAAAATCAC TGCTGTGGCC 360
ACAGCCATAT AGCTGGCACT GCCAAGTCTC ACCTTAGCCA GTGGTCAGAA GGGTCTGTGC 420
TGCGGGAGAT GAGGGCCTGC TGAGGGAGAT GAGGGCCTGC TGAGGGGCCC TGCTGTGGGG 480
GATGAGGGCC TGCTGTGGGG AATGAGGCCC TGCTGTGGGA GATGAGGGCC TGCCGTGGGG 540
GATGAGGGTC TGCTGTGGGA GATGAGGGCC TGCTGTGGGG GATGAGGGCC TGCTGTGGGA 600
GATGAGTGCC TGCTGTGGGG GATGAGGGCC TGCTGAGGGG CCCTGTTGTG GGGGATGAGG 660
GCCTGCTGTG GGAGATGAGG GCCTGCTGTG GGAGATGAGG GCCTGCTGTG GGGAATGAGG 720
CCCTGCTGTG GGGGATGAGG GCCTGCTGTG GGGAATGAGG CCCTGCTGTG GGGGATGAGG 780
GCCTGCTGTG GGAGATGAGG GCCTGCTGTG GGGGATGAGG GCCTGCTGTG GGGGATGAGG 840
GCCTGCTGAG GGAGATGAGT GCCTGCTGAG GGGGATGAAG GCCTGCTGAG GGGGATGAAG 900
ACCTGCTGTG GGAGATAAGG GCCTGTTGCG GGAGATGAGG GCCGGCTGAG GGAGATGAAG 960
ACCTGCTGTG GGGGATGAGG GCCTGGTGAG GGGGATGAGG GCCTGCTGCA GGAGATGAGG 1020
GCCTGTTGCG GGAGATGAGT ACCTGTTGAG GGAGATGAGG GCCGGCTGAG GGAGATGAAG 1080
GGCCTGCTGA GGGAGATGAA GGGCCTGCTG AGGGAGATGA AGGGCCTGCT GAGGGAGATG 1140
AGGACCTGCT GAGGGAGATG AGGACCTGCT GAGGGAGATG AAGGCCTGCT GAAGGAGATG 1200
AAGGCCTGCT GAGGGAGATG AAGGGCCTGC TGAGGGAGAT GAAGGGCCTG CTGAGGGAGA 1260
TGAGGACCTG CTGAGGGAGA TGAGGACCTG CTGAGGGAGA TGAGGACCTG CTGAGGGAGA 1320
TGAAGGCCTG CTGAAGGAGA TGAAGGCCTG CTGAGGGAGA TGAAGGGCCT GCTGAGGGAG 1380
ATGAAGATCT 1390
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