Genomic variation for the entire OR intact haplotype repertoire in 145 individuals. Every individual is represented in every locus by a single randomly selected missense allele, except for Stop loci for which the non-reference allele is preferably shown. Color coding as in Figure 3. Ethnicities: 1–53 - Asians, 54–95 - Europeans and rows 96–145 - Africans. The dataset does not include alleles with concomitant indels and CNV deletions.