chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245478671245478672CT27GENIChomozygous996032603
1245480598245480599AT21GENIChomozygous996032604
1245480625245480626CT24GENICpossibly homozygous996032605
1245482925245482926TG26GENIChomozygous996032606
1245484706245484707AG31GENIChomozygous996032607
1245484741245484742AC33GENIChomozygous996032608
1245487389245487390TC22GENIChomozygous996032609
1245487458245487459GA30GENIChomozygous996032610
1245489679245489680GT26GENIChomozygous996032611
1245500482245500483AG34GENIChomozygous996032612
1245501182245501183TA25GENIChomozygous996032613
1245501635245501636AT30GENIChomozygous996032614
1245501692245501693CT27GENIChomozygous996032615
1245507013245507014TC32GENIChomozygous996032616
1245508345245508346TC39GENIChomozygous996032617
1245508617245508618GA28GENIChomozygous996032618
1245509605245509606GA20GENIChomozygous996032619
1245510582245510583CT20GENIChomozygous996032620
1245515748245515749AG29GENIChomozygous996032621
1245516179245516180AG38GENIChomozygous996032622