chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264799436264799437AG46GENIChomozygous108636615
1264799501264799502GA47GENIChomozygous108636616
1264799734264799735TC39GENIChomozygous108636617
1264800020264800021TC43GENIChomozygous108636618
1264800263264800264CT46GENIChomozygous108636619
1264800977264800978GA31GENIChomozygous108636620
1264801211264801212AG46GENIChomozygous108636621
1264801390264801391TC51GENIChomozygous108636622
1264801637264801638TC46GENIChomozygous108636623
1264801886264801887CT39GENIChomozygous108636624
1264802030264802031CT33GENICpossibly homozygous108636625
1264802818264802819AT34GENIChomozygous108636626
1264803219264803220TA50GENICpossibly homozygous108636627
1264803636264803637CA47GENIChomozygous108636628