Tag | Content |
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EnhancerAtlas ID | HS105-52399 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr22:20776540-20778870 | 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 |
chr22 | 20777967 | 20778600 | chr22 | 20778600 | 20778659 |
| | Number: 1 | ID | Chromosome | Start | End |
GH22I020420 | chr22 | 20775061 | 20779481 |
| Enhancer Sequence | GTGTTTCTGT GTCTGGTGAT ACATGTTGTA TGTTGCAGAG TGAGTCTTTT TTTCCATTTT 60 TATGTGCGTG GTGTGGGTTG AGTGTCCTCC ATAGTAGTGG GCTGGCTGTG TGTGTGTCAC 120 AGCGCGTCTG TCTCTGTGAG CGGTGGGTTG TGTGTGTGTG TTGGAGAGTG AGTGTTTCTG 180 TCTGATGGAG TGTCGTGTGT GTGTGTGTGT TGGCAGGTGA GTGGCTGTGT TCCTCTGGGC 240 CCAGTGCTGT GTGGGCGTCT GTTGCAGTGT GTGTGCCGTC TCTGTGTTTC TGAGATTCTG 300 CTGGCTTTGT GTGTGCATGT CTGCGTTTCG GGCTGTGTGT CTGTGTTGGT GTTTCTGAGT 360 CTAGAGGAGC GTGCATGCGG CGTAGGGTTA GTGTCTGCAG GCCTCTGTGT GCTGTGGCCT 420 GCGTCTGCTT GTAACCACCA GGCTGGGCCT GGTCCCCACA TTCCTCCCAC TCCATTGTGC 480 TCTGTGCTAC AAAAAATATT TGCGTTTTCC ACCACTCATA ATTTTTCCTC CTCAATCGCT 540 ACCAGATGTG GGTCCTGTGG TCCCCATCCC CATGGCAACG GAGGTTCCAG CAGCCGCGGT 600 TCCCTTTTGT GGCGCCTGCC CTGGGAGCTG GCACTGCTGT GAGCCCCGAG GGGGTGGGGA 660 GAAGCGGGTG GTGGGAGGCA GGAGGCTGGA GGGGTCCCAG CAGCTCCCTT CCCAGCAGCC 720 ACTGGAACCC TCCTGGGGGG AAGGGAAGGC TGGTGGTAGG TTGGGGGGGG TCCCCTGTTT 780 TGTGAGGCAC CCACAGGTAG AGTCTTCGAC ACCTAGGGGG CTTCCCAGAG AAGGGCAAGG 840 AGAGGTCCCC AGAAAGGCCT GGTCACTGGG ACATCCCTGT TCTCTCCAAA TCGTGCTGGT 900 CCAGGCTGGG GGAGGAGAAA TAGCAAGAGC TGAGGGCTTG GGGGTTCAGG GAACAGCAGT 960 GTGGCATCCT CATCGTTCTG GGGGGTGGGC ACCGCCTAGA CAAGAATGTG GTCTGAGCCC 1020 CTGCACTGCC CACCCCTCAC CCACACGCAG GCACTGCCCT GCCCTCGCGG AGCCCGGCTG 1080 GGCATCTGCC CTCTTGGCCT TAACCCCAGC AGCCCGCATG GCGCAGTGCC CAAACAGAGC 1140 AGAGGCTTTC CAGCCACAGG GCCATGGCTG GGAGGGTGCC CAGCTGGCTC CAGGGAAGCA 1200 GTATGGCCCA GAGGCAGGGA TCCCACATTC CACGTGCTGC CTGTTTGTGT CCTGCCAGCT 1260 GCTCTGGACG GCCGACCCAG GGCAGGACGC AGTCTCCACT CAGATGGCTG GGCCTTCTGA 1320 GATGGGTGAC CCCTCTAAGA TGGGTGACCA AAGTTGACCT CCGTGGGGCA TCTGGTCAGA 1380 GGATGAGAGT GTGCCCAGGA CGAGAGCCCC AAGTTGCCAG CGTGAGACCA ATGAGTGCTG 1440 TGTGGCGGCT GCAGGGTGAT CAGAAGATCC TGGCAGCAGG GGAAGACTTT GAGCTGGGCA 1500 TCAAAAGATG AGATGCAGGA GAACAAGAAG AGGCCTGCCG GGCAGAGGCA GGAGGTGGGA 1560 GGAGAACAGA CAGGCAGGAG CTGGGGGAAC TTAGTGTGGG GACAGCAGGG GCCATGGAAG 1620 GTGAGGGTCT GCGGCTTAGG AGGGTCACTT AGGAGGCCTG CCCGGGAGGG TAGGCGGGTC 1680 AGGAGCAGCG AGGCCGTAGG GCACAGATGG TCACAGATAG CCAGGCAGCC GGGTCTGGCT 1740 TGGGGGCAGG GGATCTGCCC CGGGCGCTCC CTCCGTCTCC CTCAACCTTC CGCAGTAGCA 1800 GGCGGGGCTG GCAGGCAGGA GAGTTTCCGG CTGAGGACAA GGAACCCGTT GAGGCAGACA 1860 GCAGGGCTCT GTGCAGCAGG AGACCGGCTT GTTTGTGCTG GAGGAGGCCC GGCTGGAGTA 1920 AGCGCCCGCG GCCCCCTGGC CGCAGCCTCT GCACCCCCCG CAAGCTGCCA CCAACAGCTC 1980 TGAGGCCCAA GTTTAACAGC AGCGGCCAGG GGAAAAGGCC GGGATCCGAG GCAGGCCCAT 2040 CGCCTGTCCC TTTCAGTCAG GGACTCTGCC TGATCTGCCC CCACCCAACC TTCCTCCCCG 2100 TGACCAGTCC AGAATGGGGC AGGCCAGATC GGGGCCGCAT AAACTTGATA AACAAACGAA 2160 GCCTGTGGGT TGACACAGCC CACTTCCACC ATGGTCCCGG GAGACCCACG CCTGGGCTCC 2220 AGGGCTCCCC GCTGAGATAA GGGGTGGGGG AGAGTGCAGG ACAGGTCGTC ACATAAAGTT 2280 ACTTCTGGGG GGCATCTTTG GCCGAAGCCT GCAAACAGGA AGTGATCAGA 2330
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