| Tag | Content |
|---|
EnhancerAtlas ID | HS050-34171 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr19:45714790-45715870 | 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 |
| GH19I045211 | chr19 | 45715040 | 45716150 |
| Enhancer Sequence | GTCATTTTCA GAGGGCAAAG TGAGGAAGGT GCACCCTCAG GACATTCTTG CCTCAGCCTG 60
GGGAAAGAGA GTTTAAGCAA TTCCCCCAGA AAGGCACAGG AACCTCAGCC CAGAGAGGGG 120
CAGCTTCCTG CCTCGGGTCA GGAAGCACAG CCTTGGGCTC CGAGAGTCCC TCGTCTCTAC 180
CTCCCCAAGT TCAAATGTGC ATGCGTGAAG TTCCAAACCC AGCCCCAGTG CTAACCCCTG 240
GCTGCCTCCT CTTTCTGACT TCTCAGGGAA AAAAAAAAAA ACCACATACA CACAAAAAAT 300
CCCACAAGTC AGGAAACATC CATCACGGGC TGTCCAGCCC AGGCCGGAGG GGCAGGAGTC 360
AGCAGGGAGG TGACCTCAAG GTCTCCGTGG GGACTAGGAT CCGGCGGGGC TGGGGGTGAG 420
AGGCTGGAAA TTTTCCCACC CCGAGACTTT CCTGCGTCAA CCCAGGAGGG CGCCCTGGAT 480
GCCGCCAGCC CTGCCCCCAA CCTCCTTCCT CTCCTGACAG GGCAGCTTCC CGGCTAAGGA 540
TGGATGGGGA GGGTGTGCCA AGATGGAGCC ACCAGGACCA GGAATGGACA GGCACTTTGA 600
GATTGACCAG ACGAGGGACC CTGGCTCAGA GTGGCGAAGG CCTGGCCTCA GAGCCACACA 660
GCCAGGAGGT GTACATGGGT TGGCGTCGCT CCCAGCACAT GCAGCCTCCC TCTACCTCCA 720
CTACCCTGCC CAGGAGCTGG AGCCCAGCCC GGCCTTGGGT GTGTGAGAAG CCACTGGCCC 780
GGGGCCCTGC TTCCCCGGTC CTTCCTCCCC ACAACACACT CAGGACTCAG CCCTTCCTTG 840
TGTTAAATAG AAACCTCTTT ATTCTAAGTA TCGAACGTTC CTTAATACAT TGGATTGGGG 900
CCAGACCTTG AGGTGAGGGA AAGGGGCGGG GGAGCTGGGA TATTTCTGTA GAGACTTCCA 960
GAACGACACT CACCACTCTG GGCTATGGCA GGAGGGGAGG TGCTGGGAAC AGGCTTCATG 1020
GCCTTGGGAA AATGCTTTGT CTCTTTGGCC TCTGTTTCCC CCTACCTTTT TTTTTTTTTT 1080
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