Additional file 2: Figure S2. of A multi-omic analysis of human naĂŻve CD4+ T cells

Sequence variants identified in the genome and classification of SNPs in protein coding regions. (A) Total number of SNPs, insertions, deletions and substitutions identified from whole genome sequencing data. (B) Proportion of synonymous and non-synonymous SNPs identified in the coding region of the genome among non-synonymous SNPs (nsSNPs), proportion of conservative and non-conservative homozygous and heterozygous changes are shown. (C) nsSNP frequency across various molecular classes of genes. (PDF 68 kb)