Fig. 2From: Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defectsGenome-wide homozygosity mapping with significant homozygous regions on chromosome 17 marked in red for both (a) VSD cases and (b) TOF cases. The homozygosity region is present in chromosome 17 revealed for CHD manifestation.Back to article page