| Tag | Content |
|---|
EnhancerAtlas ID | HS170-01897 | Organism | Homo sapiens | Tissue/cell | RS4-11 | Coordinate | chr18:77579580-77580810 | 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 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH18I079819 | chr18 | 77579801 | 77580830 |
| Enhancer Sequence | CCCGTCCTCC CTACAGGTGA GCTGAGCGCT CAGCCAAGGA CCCGGCCAGG CCTCACAGCC 60
AGCAGGCTGC AATAGAGGCC GTCCACCTCC CCTACGGCTC CTCGGTGTGA CTGGGGTAAA 120
ATACACATCA CCTAAGGTAT TCCATTTTAA CTATTTCAAG TGGACAGTTC AGTAGCATGA 180
ATTCCAACCG CCGTGCTGTG CAGGCATCAC CACTTTTTGC CAAATTCTTC CATTGCCCTC 240
AACAGGAAAT CTGTAACCAC TAAGCAGTAA CTCCCCCATA GTGCCACCTC CAACCCCTGG 300
TAAGGTCCAC TCTGCTTTCT CTATGAACCC CGCTATTCTA GGGATTTCAT GTAGGTGAAT 360
CACACAGTGC TGGTCCTCCA GTGTCCAGCT TCTCTCACTC AGCATAACGC TCTCCAGCTC 420
CAGCCGCGCT CCGAGGAGGA GCTCCTTCCT TCTCCGAAGG AGGTGCGTGT CAGAACCTCC 480
TCCTATTCTG TGTCTGGGCA GTGCCCTCGT GCAGGGTACC CCACACTGTG TGCGTCCACC 540
CTCTGTTGGC GACACGTGGG CTGTCCCCAT CATTTGGCTA ATGGGACTGA TGCTGCTCTG 600
AACGTCGGCG CTTGTATCCT CTGTTTGAGT CCCTGTTTTC ACTTCCTCCC CACCTTTTGG 660
CTAATGGGGC TGATGCGGCT CTGAATGTCA GCACATGTAT CCTGTTTGAG TTCCTGTTTT 720
CACTTCCTCC AGGCATGTTC TTAGGAGGGA AATGCTGAGC CAGATGTTGA TGCTGCTGCT 780
TAACTTTTAG AGAGTCTGCC AAACTTCCAC AGCAGCTGAG CCATTTTCCC ATCGGCAATC 840
CTGAGGGGTC CAGTATCTCC CATCCTCACC AGCACTCAGG ATGGTCTGTC TTTCTTATTA 900
CAGCCATCCT GGCAGATGTG AAGCGATAGC TCATATCTGC ATTTTCCTAA TGATGAGTGA 960
TGCTGAGCAT CTTTTCATCT GCTTGCCGGG CATGTGTGCA TCTTCTTTGG AGAAAAGTCT 1020
GTTCAAATGG GTACAATGTA CATTTTTTAA AAAAAGGCTA TTCAAGTTCT TTGCCCATTT 1080
TATTTACTTA TTTATTTAGA GACAGGGTCT CACTCTGTTG TCCAAGCTGG AGTGCAGAGG 1140
TGCAATCAGC CTCAACCTCC TAGGCTCAAG CAATCCTCCC ACCTCAGCCC CTGGAGCAGC 1200
TGGGACTCCA GGCATGCACC ACCACACCCA 1230
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