| Tag | Content |
|---|
EnhancerAtlas ID | HS050-50317 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr4:3451220-3452410 | SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACGCTGCCT GGCCCCTGCC TGCGGCCCCG CCTTCCCCTC CAGGCCATGA CTGGGGCCCA 60
GGTCTATGCG CAGCAGGCCT CAGGCTGCCG TTCTGGAGCG CACACAGTCC TCAGTGGAGA 120
CGGAGCCTGT GGCCCCACAG CGGGGTCTGG CCCCACGGCC CAGAGAGTTG TCAGGGGATG 180
AGGTCTGGGC CTCTCCAGGC CCCAGCAGAG TCCAGCCCCC TCCCAGGCCA GCCCCAGGCC 240
GGGGCTCAGC ACCTGGGTTG TCCCAGGGCA GGAAGTGGAA ACCAAGTCCA GGCCCCCAGG 300
CGTGGAGGGG TCCGATCCGC GTGGTGCACG GAGTATTGAA CCTGAAGAAG AAAGAGCGGC 360
CCCACGGGAA CACCCGCAGG CCGTCGTTGG TCTTCCAGAT GGCAGCCCGC CTGCCTGAGC 420
CTGGGCTGCA CTTCCCGGGA GGGAGGAGGC CACAGGCTGC CTCTGTGGGG GCTGAGGGAG 480
GGAGGGGCCC ATGTGCTAGA TGGGGCCCAG TTAGAGGGTC ACTGCTGGGC AGGCAGAGGC 540
CGTACCCTCC CTCCAGCCAG GGAGGACAGG AGACAGGGGG AGGTGGGGCC AGAGGGCAGA 600
GAGGGCGGGA GTGTGGCTGG TGGGGGTCAG GCCTCCTCCC TGCTTCGAGG CACCCAGGAC 660
CTTCTCTCCT GCGCCCCACC TCCTTCCTGG CGTCCTGGTC TCGGGGAGGC AGTGGTTTGC 720
AGTTACAGCT GTTCCCTTTC GTCGGGAGCC CCTTCCCCAG CAGATTGGCG CCGCCCCAGG 780
CTGTACGGAG GCTGGGAGGG CAGGAAATGG GGCATTGGGG CCACACAGTT ACCGCCCCAA 840
GCAAAGCCGG GTTCTGAGCA AAGAGGGAAG AGAGACATGG CCAGGCCCTT CTCCCCACGG 900
CCCCTGCTGC TGTGCATGGG CCTCAGAGCC TTCGAGCTCA CGGAACGAAC TTGCCACTGA 960
AGACCCCTGC CCCTGCCACA GTGTTGGTGC AGCCTGGGCA GTGGCTGGGG GACTGAGTCT 1020
GGCACCTGTG CCCCAGGATC CTGAGAGTGG AGCCGCTCTT CCTCCTGAGT GTGGGGGCCT 1080
CCAGCAGCTG GTTCTGGGGC TCTGAACCTC ATGGCTTCAG CCCCGCTTCA CCCACATCCG 1140
ATGTGAGCCG TCCCTGACCC TTCCGCCATG AGCGGTGAGC ATTTTCACAT 1190
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