chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 8,117052890,117052891,A,G,40,GENIC,heterozygous,926419056 8,117054122,117054123,C,T,20,GENIC,heterozygous,926419057 8,117054158,117054159,A,G,20,GENIC,heterozygous,926419058 8,117055685,117055686,C,T,20,GENIC,heterozygous,926419059 8,117056327,117056328,C,A,69,GENIC,heterozygous,926419060 8,117056459,117056460,G,A,61,GENIC,heterozygous,926419061 8,117057218,117057219,T,-,42,GENIC,heterozygous,926453168 8,117058388,117058389,A,G,45,GENIC,heterozygous,926419062 8,117059204,117059205,A,C,54,GENIC,heterozygous,926419063 8,117060807,117060808,C,T,32,GENIC,heterozygous,926419064 8,117061256,117061257,C,T,57,GENIC,heterozygous,926419065 8,117061986,117061987,C,T,11,GENIC,heterozygous,926419066 8,117062340,117062341,T,TGTCA,35,GENIC,heterozygous,926453169 8,117062839,117062840,C,G,67,GENIC,heterozygous,926419067 8,117067190,117067191,G,GCTGT,24,GENIC,heterozygous,926453170 8,117067250,117067251,A,G,26,GENIC,heterozygous,926419068 8,117067587,117067588,T,C,19,GENIC,heterozygous,926419069 8,117068510,117068511,A,G,44,GENIC,heterozygous,926419070 8,117068680,117068681,C,A,34,GENIC,heterozygous,926419071 8,117068800,117068801,A,G,36,GENIC,heterozygous,926419072 8,117068936,117068937,T,TTC,14,GENIC,heterozygous,926453171 8,117074996,117074997,A,G,38,GENIC,heterozygous,926419073