Fig. 3

Views from the UCSC genome browser depicting SNP information derived from whole genome sequencing of samples from the Iranian (Ira_AH) and French (Fra_MC) populations. Comparison of the Xpr1 introgression region (top - genome position chr1:154,900,000-155,900,000) with the previously described introgression of the Vkorc1 region [47] (bottom - genome position chr7:123,000,000-133,000,000). Three tracks are shown for each population, the top one is based on SNP polymorphisms (vcf files) with the haplotype sorting function of the browser activated. The second represents the scores for nucleotide diversity and the third is Tajima’s D, both calculated across successive 1 kb windows. The scale is shown on the top, the RefSeq genes are at the bottom of each view. The focal genes are highlighted in yellow