List of the 73 variants selected for validation.

Abbreviations: Chr, Chromosome; Ref, reference allele; Obs, observed allele; HOM, homozygous; HET, heterozygous; Func, variant function; SNPs, single nucleotide variants/polymorphisms; MAF, minor allele frequency; GoNL, Genome of the Netherlands project database, 498 unrelated Dutch individuals; EVS_EA, NHLBI Exome Sequencing Project database, 4,300 European-American unrelated individuals; 1000G, 1000 Genomes Project, 2,500 individuals from about 25 populations around the world; GIFT, Genetics In Familial Thrombosis study, 96 unrelated VTE cases with positive family history of VTE; GoNL, Genome of the Netherlands project database, 498 unrelated Dutch individuals.