Promoter region SNP position SNP ID Gene Disease Type P-value Source
chr9:119449581-119463579 chr9:119462112 rs3019 TRIM32 Coronary heart disease UTR-3 0.00039 GWASdb
chr9:119449581-119463579 chr9:119461680 rs17637172 LOC105376250 Cognitive decline rate in late mild cognitive impairment intergenic_variant 2e-07 GWAS_Catalog