| Tag | Content |
|---|
EnhancerAtlas ID | HS193-22166 | Organism | Homo sapiens | Tissue/cell | U87 | Coordinate | chr22:31044830-31046150 | 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 |
| GH22I030648 | chr22 | 31044758 | 31046162 |
| Enhancer Sequence | AAAAAAAAAA AGGGCTGATG AGGGTCTTGA CAAGGGACTG TGCTCAGGAG GCTTGCAGGG 60
GTATAGGGGA GCAGGGCTCC CATGTAGGGA ACCTAAGACA GGAGTCCCAA CCCCCAGAGC 120
TCCCTGACTC GCCAGCTGGC GTCAGCTTTG TTATTTACCT CTGAGCCTTT CCTTGGCTCT 180
TGTAACACCT AACTCTCCCC AGCCAGCTAC CTCTCCTGGA GATCACCTGT TAAAGATGAT 240
AAGGACCCAG TTGGAGTGAG AACACCTGGA ACCTAATCCT GCTCTGCCCA CCTGACTGGG 300
AGCCTCCCTT CCCTAGGCCT CAGCTTCCAG ATCTGCAAAA TGGAACTGAT GATCCCTATG 360
GAGAGGGTTC GAATGAGGAG CGCTGGGCAG GGCCAGGAGT GAGGAAGGAG GTAATGGCAC 420
CAACTGGCTC TGCTTTTATC TTGGGGTATT CACCCAACCT TTCTGGAAAC CATCTGCAAA 480
ATGTCTCCCA TTTGTGTGAG GACTAGGAGC TAGACCAGGC TGGGGCTGTG GTCTATGGAG 540
ACTGAGATTC AGGGAGGAAT CATTCAGATT CAGTAACCAG AATTCGTAAG GGACCACAGT 600
GCCAGCAAGT GCTAGACAGG GCTGAGTAAA GGGCCAGCCC ACGGCGGGGT GGGAGTGGGT 660
AGGGAAGGCC TAGGAGGACC GGTATGGGGT TTCCTGGTTC CAGCCTCCGC CCAGGCTGCC 720
TTACAGAAGG GGAAGTCGGC CTGGGCTGAG TCACCTGTCA CCCACCCTCT CTATGACTCA 780
GAGATGCCGC TGGCCCAGCC CAGTCCCTGA GCAGCTTGGG TACCTCTGGC CTCCACTCTC 840
AGGCTTTGCC AGGCAGGATG GAGGGATGGA TGGCTGTGGT CAAATCCTCC TCGGTGACTC 900
AGGACCCTTT CCCATCCAAC TGGCCCCCAC TGCCATAGCA GGGACCTCCC TGTACCACCC 960
TCATTTCTAG GCCTTGTGGG ATGCTTGGCT AATGAGTGAG CCTCACATCA GATTAAAGCC 1020
TGCCCCTGGT GGTTGTGGGG ACAGGTAATT GGGGTTGTGT GTGACCTGGG AGCTGGTTTG 1080
TCACCAGATT CAGGACCATT AGACATTGAG GTGATTCCCC CAAGGCCACA GCCAAAGCCA 1140
TGCCTATCAC CCCTCCCAGC AGTGGGCACA GAGAGCGCTG GATTGGGAGT CAAAAAGCTT 1200
GGGTTTGGTG GGATGTGGTG GCTCACGCCT GTAATCCCAG TACTTTGGGA GTCCGAGGGG 1260
GGCGGATCAC CTGAAGTCAG GAGTTCAAGA CCAGCCTGGC CAACATGGTG AAACCCCGTC 1320
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