Whole-genome sequencing data from 100 blood samples that have been collected from a reference cohort reflecting the general Belgian population. A matrix containing Single Nucleotide Variants (SNVs) identified in a sample of 100 BELHES participants. The file is a CSV file with one line per sample (pseudonymised ID) and one column per variant. Column headers are chr:position. Reference genome version used was GRCh38.
