chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,114216049,114216050,G,GT,13,GENIC,heterozygous,925701397 X,114216077,114216078,C,CCT,13,GENIC,heterozygous,925701398 X,114216078,114216079,T,C,13,GENIC,heterozygous,925695779