| Tag | Content |
|---|
EnhancerAtlas ID | HS050-50356 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr4:4992190-4993980 | 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 |
| GH04I004990 | chr4 | 4992141 | 4993979 |
| Enhancer Sequence | TTGCCTCCGC AAAGTTTTAG CCTCCTGGTG AGTGCTGGCT GGATCCAGGC TTGGTGTAGG 60
GTGGTGAAAG AGCACTGGAT AGGGGGTTAG ATGACTAAGC CTGCTGTGTG ACTTCCAGCT 120
GGTTGCTTAA CCTCTCTGGG CTGCACTTTC TTCCTCCATG ATAGGAGAGG GCTGGATTGG 180
GTTAGGGATG GCACAGTCAA TGCCTCTAGG TGCCAGCAAG GTGATGTCCA TGTGTGATGG 240
CCCTGTGTAA AACACCCTCG ACCTCCATGG GGTCAAGCCA GGGCTTGTGG CCTCCCATTC 300
TTGTCCACAT CCCGACATAA AAACTTAGGC ATTTTTTTTC TTTTTTCCTG TAGAACCTCA 360
CAAGAATATT TTGGAAACAA GACAAAGAGG GAGGATGCTG TTGGCTGTAG CTCAGAGCTT 420
CTCAACACAG GGCTGATTTG GGCCCTGATT TGGCCATGTC TGGGGCGTTT TTGGCTGTCA 480
TGACTGGGCC ATCATCTGGT GATGCTGCTG ACATCCTGTG GGTGGAGGCC GGGTCTGTGG 540
CTAAACACCC CACAGTGCAA AGCCCCACCA CCGACAAAGG ACTAGGTGGC CCCAGACGCC 600
CCCAGTGCCC AAGGCTGAGA GCCCTGCAGC AGGGCGGGGT TGGGTTGGAT TTGGGAGTGG 660
AGACTGGCTG GCCTGGGTGG GTCCCTGCCA CTGGCTTGAC ACCCTGTGAT GCAAAGCAGT 720
GCCCGTGGAG CCTTGGATCG CTGGCTGTCA GCCACATGAG TCAGCAGGGC CCGAGCACAG 780
CCTCCATGCT CTCTGGCTGT GATGGGCCTA CAGACTGACC TTTGTCAAGG GCTGGAGAAC 840
CTCGGACGGC TGCCACCAAG CCCCAGGCAG AGCCTAAAGA TTTGTCAGGG TTGGGGGTGG 900
GGGACCAAAG ATGCTGGTTA AGTGTTGAGG AGTGAGGAAG CCACAGTGAC TAAGCCGCGC 960
CTGGGCGCCG CGGGCTGATC CTAATGAAGC CTAGCCAGTC TCTCCTCCAC AGTTTTGACA 1020
CAGTTAGAAA AACTTTCTCT TGTTTAACTG GAAACAGCCA CCCACACTCA CCCTTTCACA 1080
TACCAGTTGC CTTCTTGCAG ATCATAGGAA ATAAACTGAC CTTTTAAAAA ATCACAAGTG 1140
AAATATAAGG AAACAGAGTG AGCGGAGGCG TTTAGGGGTC TTGAATTCGG CCCACTGGGC 1200
AGGAGTGAGC AGGAGTGAGA TATGTGAGGC TGTGTGAGTC CATCCTGCCT CCACTCTCTG 1260
TGCTCCCGTC TGTGGAGTGG GGCAGTGGAC ACGGGCTCCT CAAGCCTGCT GGCTCTCTCG 1320
GTTTAGGTGT CTCCTGACGG GAGTGGGAAT CCGGGCAGGG GCGGGTGGCT GCTTCTCAGG 1380
GCCTTCTCAC GGCTCCCTTC TCGGGACATT TCATTCACAG ATTTGTGAAT CTGCAGTTTT 1440
GGGAGGATGA CTAAAGGTCA CTTTGTCCAA CCTCAAATGC AGATATGCCC TCTACTTTCT 1500
TCCCAAGAGG TAACATTGTC TCTCCTTGGT GGCTCCTGGG ATGAGGGGCT TACTCCTATG 1560
CCCAGGCCAG CCAATTTCAT TCCTGGACAC CCCTGGACAG CTCTCGCTTC CGTGCGTGCT 1620
GTTTTTTTTT TCCTTTTTTC TTTTTTTTTT TTTTTTGAGA CAGACTCCAG CCTCGCTCTG 1680
TCGCCCAGGC TGGAGTGCAG TGGTGCCATC ACCACTCACT GCAACCTCGT CCTGCAGACT 1740
CAAGCGATCC TCCCACCTCA GCTGGGATTA CAGGCATGTG TTACCACACC 1790
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