chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109010968790109688CT24GENIChomozygous116951136
109011151790111518TC32GENIChomozygous116904235
109011660790116608TC48GENICpossibly homozygous116951138
109011957890119579CG26GENIChomozygous116904261
109012561390125614AT18GENIChomozygous116904269
109012592390125924AG29GENIChomozygous116904271
109012664290126643AG27GENIChomozygous116904273