Among these, 14 genes (CD3G, SCARB1, MYO5A, RABEPK, KIF2C, EXOC7, COPG2, REPS1, NFYC, SYK, EEA1, CARD9, DNASE1, TAC1 and RHBDD3) were significantly enriched for immune related pathways, including vesicle-mediated transport (p = 1.32 × 10−3), regulation of acute inflammatory response (p = 4.76 × 10−4) and tuberculosis (p = 2.53 × 10−3) (Figure 2B). This evidence concerns the gene DNASE1 and tuberculosis.