chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 47604193 47604194 A G 49 GENIC homozygous 813538050 13 47604294 47604295 T C 52 GENIC homozygous 813538051 13 47604483 47604484 C T 34 GENIC homozygous 813538052 13 47604490 47604491 C T 35 GENIC possibly homozygous 813538053 13 47604629 47604630 A C 42 GENIC homozygous 813538054 13 47604888 47604889 T C 16 GENIC homozygous 813538055 13 47605725 47605726 G A 17 GENIC homozygous 813538056 13 47605764 47605765 G T 19 GENIC homozygous 813538057 13 47606154 47606155 A T 34 GENIC homozygous 813538058 13 47606901 47606902 C T 28 GENIC homozygous 813538059 13 47606905 47606906 G A 28 GENIC homozygous 813538060 13 47606934 47606935 A G 29 GENIC homozygous 813538061 13 47607019 47607020 A G 23 GENIC homozygous 813538062 13 47607027 47607028 G A 24 GENIC homozygous 813538063 13 47607282 47607283 G T 24 GENIC homozygous 813538064 13 47607289 47607290 C T 25 GENIC homozygous 813538065 13 47607530 47607531 G A 26 GENIC homozygous 813538066 13 47607534 47607535 G T 24 GENIC homozygous 813538067 13 47607591 47607592 G C 31 GENIC homozygous 813538068 13 47607616 47607617 G A 30 GENIC homozygous 813538069 13 47608132 47608133 T G 28 GENIC homozygous 813538070 13 47608281 47608282 A G 30 GENIC homozygous 813538071 13 47608742 47608743 A G 30 GENIC possibly homozygous 813538072 13 47609111 47609112 T A 24 GENIC possibly homozygous 813538073 13 47611073 47611074 A G 18 GENIC homozygous 813538074 13 47611158 47611159 C T 36 GENIC homozygous 813538075 13 47612899 47612900 G A 20 GENIC homozygous 813538076 13 47614924 47614925 G C 4 GENIC heterozygous 813538077