chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1174565963174565964AT47GENICpossibly homozygous145314085
1174566042174566043AG49GENIChomozygous145314086
1174566310174566311TC57GENIChomozygous135752097
1174566762174566763CT57GENIChomozygous145314087
1174566922174566923TA9GENICheterozygous144571082
1174567770174567771CT42GENIChomozygous145314088
1174568071174568072GA37GENIChomozygous145314089
1174570463174570464AC37GENIChomozygous145314090
1174570475174570476AC38GENIChomozygous135752098
1174570986174570987AC47GENIChomozygous135752099
1174572377174572378T42GENICpossibly homozygous141133997
1174574158174574159AG49GENIChomozygous141277069
1174575280174575281GA40GENIChomozygous135752101