chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146973704146973705GA11GENIChomozygous112873811
4146974069146974070CT16GENIChomozygous112873813
4146977067146977068TC14GENIChomozygous113180142
4146977287146977288GA23GENIChomozygous113180143
4146978280146978281TG13GENIChomozygous113180144
4146978295146978296CT10GENIChomozygous113180145
4146978480146978481CG7GENIChomozygous113180146
4146978901146978902CT11GENIChomozygous112873818
4146979045146979046TG40GENIChomozygous112873819
4146979541146979542TC8GENIChomozygous112873821
4146979926146979927CT9GENIChomozygous112873822
4146979928146979929AG8GENIChomozygous112873823
4146980245146980246TC21GENIChomozygous112873824
4146980424146980425TC11GENIChomozygous112873825
4146980437146980438CT9GENIChomozygous112873826