Tag | Content |
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EnhancerAtlas ID | HS024-11336 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr22:50178960-50180220 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH22I049784 | chr22 | 50178434 | 50179657 | GH22I049786 | chr22 | 50179761 | 50179910 |
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Enhancer Sequence | CAAACCCCAG CCCCACGGCC GGCAGGGCCT CCACGCACGC AGCCCCATAC CTCTGCCGCC 60 GACAGACGTG AAACCCCGAG GAAGTGGAGC GTCAGCCGAA CTCCAAGTTC TGCATGCAGA 120 GGGGACGCCC ACAATTACAC TGACCCAACC TCTAGTACCC AGTGCACAGC ACCCTGACCC 180 GATTCATCAC AGAATTTCCG GGGTGCTTGG AAAACCAGGT CAGAGTCTTT CACCAAAGGT 240 GGCTAAGAAA GACCAACGTG GTTAAGACAC ATCCCCCAGT CCTGAGTCAA GGACATCTAT 300 TCTTATTGGT ATCTTGTGAA ACATTTCAAT AGCTTCCTAT TACTTAGAAA GCAAAAAAGC 360 TTTTTCAAAT TATTTTAAAA TGCCAATTTA ACATCAATCC ATCAAAGTAA AAGGACATGG 420 GTAGAAAATT TCTACACATT CAGTTACGTG CAAAATTTTC ATACAAATCA AAATGAAATT 480 TACCAGAAAT TACTTTGGCA ACAAGACGCA TGACCTGCTT GCTGGCAAGG GTAGGAAGTG 540 AGCCTCCTTC TGCACAAAGA CCTTTGACAG TGCCTGGTCT CACTCCCCTC CCCGGACGCT 600 TCAGGCCAGA GACCAGCAGA AGGAACAGGG ACAAGATGTG AGGGAGTGGC CTGGGCAGGT 660 CTTGCCCACC ACAGCCTTCC ATCTGCACCC GGCCTGGTGA GGCTCCATGA CACAGGACTC 720 ACTTGCTGCC ACTCTGGGAA ATAAGCAACA CCCACCCAGC CCCACCCTCT CTCACTGCTC 780 AAGTGCACGA GGCACCACGG CACACCAGCA CAGCCAGGAG AAAATGCGCA TCTCCTTATC 840 TAGGTATAAC AGGCAGACAG GACAGACGGG AACCAAGCCT TGACTCGGGA CAAAAACCAA 900 AATGACAAAC ATGCTCCAGA CACGCTTCCA GAAAAGAGTC GCTGGCAACC TGAGCCGGCA 960 CCTCCAGAAG CGCAGCCAGT ACCGAAGAAG CAAACCGATG ACAGCTGCTC CTCTTTAAAG 1020 GACAAACTCC TCAGCTTCCT CTGAGGGGCG GGGAGCAGAG GCTGCAGGAA CACAGCGGCC 1080 TCCTCAAAGT GCTCCCAGCA CAGCACACAC ACGGCAACAC CCTCACCGAG GAATTCAACA 1140 GAGTTCAGTT ACAAAAGCGC AGCAAGAGAT GAGAAGCGCT TTCCAGTGCT ATTTCAGCAG 1200 GTCCTAATAC CTCATCACAT ATGTGGCTAA GAGGGCCACA TAAAACAATG AGTAAATGTT 1260
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