chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 117052068 117052069 A G 15 GENIC heterozygous 926609932 8 117052890 117052891 A G 21 GENIC heterozygous 926609933 8 117054122 117054123 C T 20 GENIC heterozygous 926609934 8 117054158 117054159 A G 30 GENIC heterozygous 926609935 8 117055685 117055686 C T 9 GENIC heterozygous 926609936 8 117058726 117058727 C T 60 GENIC heterozygous 926609937 8 117062340 117062341 T TGTCA 55 GENIC heterozygous 926646800 8 117065011 117065012 A G 39 GENIC heterozygous 926609938 8 117066348 117066349 C T 18 GENIC heterozygous 926609939 8 117066426 117066427 G A 14 GENIC heterozygous 926609940 8 117067190 117067191 G GCTGT 41 GENIC heterozygous 926646801 8 117067250 117067251 A G 40 GENIC heterozygous 926609941 8 117067587 117067588 T C 14 GENIC heterozygous 926609942 8 117068680 117068681 C A 39 GENIC heterozygous 926609943 8 117068800 117068801 A G 47 GENIC heterozygous 926609944 8 117068936 117068937 T TTC 34 GENIC heterozygous 926646802 8 117071534 117071535 C T 29 GENIC heterozygous 926609945 8 117071896 117071897 G A 29 GENIC heterozygous 926609946 8 117072006 117072007 C T 20 GENIC heterozygous 926609947 8 117072252 117072253 A AG 19 GENIC heterozygous 926646803 8 117072978 117072979 A G 19 GENIC heterozygous 926609948 8 117074996 117074997 A G 51 GENIC heterozygous 926609949 8 117075165 117075166 A G 10 GENIC heterozygous 926609950