Supplementary tables for GWAS in patients with iSSNHL

Supplementary Table S1: Genes within ±250 kb of each genome-wide significant lead SNP (GRCh37/hg19; NCBI37.3.gene.loc).Supplementary Table S2: Cleaned gene set derived from suggestive loci (Table 2).补充表S1：每个全基因组显著性先导单核苷酸多态性（single nucleotide polymorphism, SNP）上下游±250kb范围内的基因（基因组版本为GRCh37/hg19；注释文件为NCBI37.3.gene.loc）。补充表S2：源自提示性关联位点（表2）的经清洗基因集。