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