Tag | Content |
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EnhancerAtlas ID | HS050-40676 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:239412570-239413920 | 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 |
chr2 | 239412892 | 239412967 | chr2 | 239413457 | 239413602 |
| Enhancer Sequence | TCTGTCCTTT TACTACCTTT ACAAAAACCA CTTTTGCAAA ACAGTAGAGA GAGTTCAAAT 60 TCTAAAGTGA GGGAGGGGTG GATTGAGGAG CAGATTGCCC AGTTTGTCCA CAGATCTTCA 120 TGCTATTCTG CATCTGCTGG GAGTGGGAAA AGCTTGGGGG CTGCCACCCC TGAGGATCAG 180 ATATTTATGT GACAGATGAA CCCTCCTGCT AACGCTGCTG TATTGAAAAG TCCCAAGAAA 240 GAGCAGTCCC AAAGGGAGTC CAGCTGGGCC CTGGGACCTG CACTGATCCC AAAGCTGCCT 300 AAAAGAAAAC GCCTGGGGCG CACCTATAGC TCCAGGAGGA AAATGGCCAA GGGCGCGCAG 360 CAGACTGCCG ATGGGAAACA CCTGTTCTCC GGGCTCGTGG GGGCTGGCCA GGCATTGTTC 420 TCTATTTGCG TGTTTTGCTT TCAGCTCATT CAAACTCAAT ATAGTGGTGA AATTAAGTAC 480 ATCATCAACC TAAAGCTACC AAACCAAATA CATAAATGGA AGGATTTGAA AAATCTGTAA 540 TAGCTGGGGT GAGGCTGGCC TCGGGCCAGC TGGGCTGCCC GGACAATGGA GGCAGTATGA 600 GTGCTTGGGC CACAGCGGGA GGGCGAGTTT CCACCCCGGG GTGGCCTGGG GATCTGATCC 660 AGCCTGAGGA AGGGCTTGGG TGGAGCCCCG AGGGGGCTGG AGGGCTGCCG GGGTGGGGGG 720 GCTCTAACCT GCAGACGTGA GCCCCCAAAG CCGGCTGTCA TCATGCGGGC CGCGGGGGGA 780 GCCATGCTGT GTGGGAAGCA GGGGCGGTGG GATCCGGAGG GGGAAGGTGT GGAAATTTGA 840 CACAAACGCA AATGTTTTAC CTTCTAAATC ACCTTGGTCT TGCAGTTGAA AATTCTCCCT 900 GAACTTCCCA CCCCAAATGT CTCAGGGAGG GGGAATCTGG GCAGCTTCTC GCTTTCCAAA 960 GTCACAAGTC ATAATTCTTT CTTCCTGCTG CAACCGGCGC AGGCTGAGTT CTGAATGTGG 1020 TGCTGAGATG GTGTGAAAAT CTCCGAGAAT ATCTGGGGAC CTTGCACCTC CACCCCCACC 1080 CAGACCCCGC AGTGACTGGG TGGACTTTCC AAGGCGGTTC CGTTTGGGGT TCTGCGCTCC 1140 TAAGGAACTC TGTTAGCCAG GAGGGCCAAG GCCCCTGCGC CCTCAGATGT GATTCACTGA 1200 CCACCTTCAG CCTAAAATGG CTTTGGAGAG CTGGAGGCCA GGTAGTGTGT TGACCGAGGC 1260 CACACTGAGC ACCCCTCACA TCTGCCCTCT GTGCAATGCC TGTGCACACT GGTCACTGTG 1320 GCTTCCAAGG AGCCGGCCTC CTTTCACTGC 1350
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