Tag | Content |
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EnhancerAtlas ID | HS050-44127 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr22:20776200-20778870 | 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 | CTCCCGGGTT CAATCGATTC TTCTGCCTCA GCCTCCTGAG TGGCTGGGAT TACAGGCGTC 60 TGCCACCACA CCCAGCTAAT TTTTTGTATT TTTAGTGGAG ACAGGGTTTC ACCATGTTGG 120 CCAGGCTAGT CTTGAACTCC TGATCTCAAG TGAACCGCCT GCCTCGTCCT CCCAAAGTGC 180 TAGAATTACA GGCGTGAGCC ACCGTACCCG GCCGCACGTG TATTTTGTAT GATATATATC 240 TGCTTCTGAC TTTGGTGAAG TGTGTGTGTC GCAGGGTTGT GTCTATCTTG TGGTTTCTAT 300 GTGGCCTATG GTGTGTGTGC TGCAATGAGT CTCTGTCTTG GTGTTTCTGT GTCTGGTGAT 360 ACATGTTGTA TGTTGCAGAG TGAGTCTTTT TTTCCATTTT TATGTGCGTG GTGTGGGTTG 420 AGTGTCCTCC ATAGTAGTGG GCTGGCTGTG TGTGTGTCAC AGCGCGTCTG TCTCTGTGAG 480 CGGTGGGTTG TGTGTGTGTG TTGGAGAGTG AGTGTTTCTG TCTGATGGAG TGTCGTGTGT 540 GTGTGTGTGT TGGCAGGTGA GTGGCTGTGT TCCTCTGGGC CCAGTGCTGT GTGGGCGTCT 600 GTTGCAGTGT GTGTGCCGTC TCTGTGTTTC TGAGATTCTG CTGGCTTTGT GTGTGCATGT 660 CTGCGTTTCG GGCTGTGTGT CTGTGTTGGT GTTTCTGAGT CTAGAGGAGC GTGCATGCGG 720 CGTAGGGTTA GTGTCTGCAG GCCTCTGTGT GCTGTGGCCT GCGTCTGCTT GTAACCACCA 780 GGCTGGGCCT GGTCCCCACA TTCCTCCCAC TCCATTGTGC TCTGTGCTAC AAAAAATATT 840 TGCGTTTTCC ACCACTCATA ATTTTTCCTC CTCAATCGCT ACCAGATGTG GGTCCTGTGG 900 TCCCCATCCC CATGGCAACG GAGGTTCCAG CAGCCGCGGT TCCCTTTTGT GGCGCCTGCC 960 CTGGGAGCTG GCACTGCTGT GAGCCCCGAG GGGGTGGGGA GAAGCGGGTG GTGGGAGGCA 1020 GGAGGCTGGA GGGGTCCCAG CAGCTCCCTT CCCAGCAGCC ACTGGAACCC TCCTGGGGGG 1080 AAGGGAAGGC TGGTGGTAGG TTGGGGGGGG TCCCCTGTTT TGTGAGGCAC CCACAGGTAG 1140 AGTCTTCGAC ACCTAGGGGG CTTCCCAGAG AAGGGCAAGG AGAGGTCCCC AGAAAGGCCT 1200 GGTCACTGGG ACATCCCTGT TCTCTCCAAA TCGTGCTGGT CCAGGCTGGG GGAGGAGAAA 1260 TAGCAAGAGC TGAGGGCTTG GGGGTTCAGG GAACAGCAGT GTGGCATCCT CATCGTTCTG 1320 GGGGGTGGGC ACCGCCTAGA CAAGAATGTG GTCTGAGCCC CTGCACTGCC CACCCCTCAC 1380 CCACACGCAG GCACTGCCCT GCCCTCGCGG AGCCCGGCTG GGCATCTGCC CTCTTGGCCT 1440 TAACCCCAGC AGCCCGCATG GCGCAGTGCC CAAACAGAGC AGAGGCTTTC CAGCCACAGG 1500 GCCATGGCTG GGAGGGTGCC CAGCTGGCTC CAGGGAAGCA GTATGGCCCA GAGGCAGGGA 1560 TCCCACATTC CACGTGCTGC CTGTTTGTGT CCTGCCAGCT GCTCTGGACG GCCGACCCAG 1620 GGCAGGACGC AGTCTCCACT CAGATGGCTG GGCCTTCTGA GATGGGTGAC CCCTCTAAGA 1680 TGGGTGACCA AAGTTGACCT CCGTGGGGCA TCTGGTCAGA GGATGAGAGT GTGCCCAGGA 1740 CGAGAGCCCC AAGTTGCCAG CGTGAGACCA ATGAGTGCTG TGTGGCGGCT GCAGGGTGAT 1800 CAGAAGATCC TGGCAGCAGG GGAAGACTTT GAGCTGGGCA TCAAAAGATG AGATGCAGGA 1860 GAACAAGAAG AGGCCTGCCG GGCAGAGGCA GGAGGTGGGA GGAGAACAGA CAGGCAGGAG 1920 CTGGGGGAAC TTAGTGTGGG GACAGCAGGG GCCATGGAAG GTGAGGGTCT GCGGCTTAGG 1980 AGGGTCACTT AGGAGGCCTG CCCGGGAGGG TAGGCGGGTC AGGAGCAGCG AGGCCGTAGG 2040 GCACAGATGG TCACAGATAG CCAGGCAGCC GGGTCTGGCT TGGGGGCAGG GGATCTGCCC 2100 CGGGCGCTCC CTCCGTCTCC CTCAACCTTC CGCAGTAGCA GGCGGGGCTG GCAGGCAGGA 2160 GAGTTTCCGG CTGAGGACAA GGAACCCGTT GAGGCAGACA GCAGGGCTCT GTGCAGCAGG 2220 AGACCGGCTT GTTTGTGCTG GAGGAGGCCC GGCTGGAGTA AGCGCCCGCG GCCCCCTGGC 2280 CGCAGCCTCT GCACCCCCCG CAAGCTGCCA CCAACAGCTC TGAGGCCCAA GTTTAACAGC 2340 AGCGGCCAGG GGAAAAGGCC GGGATCCGAG GCAGGCCCAT CGCCTGTCCC TTTCAGTCAG 2400 GGACTCTGCC TGATCTGCCC CCACCCAACC TTCCTCCCCG TGACCAGTCC AGAATGGGGC 2460 AGGCCAGATC GGGGCCGCAT AAACTTGATA AACAAACGAA GCCTGTGGGT TGACACAGCC 2520 CACTTCCACC ATGGTCCCGG GAGACCCACG CCTGGGCTCC AGGGCTCCCC GCTGAGATAA 2580 GGGGTGGGGG AGAGTGCAGG ACAGGTCGTC ACATAAAGTT ACTTCTGGGG GGCATCTTTG 2640 GCCGAAGCCT GCAAACAGGA AGTGATCAGA 2670
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