chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265290448265290449GA16GENIChomozygous108636938
1265290684265290685AG23GENIChomozygous108636939
1265290865265290866TC10GENIChomozygous108636940
1265291237265291238TC28GENIChomozygous108636941
1265291484265291485TC24GENIChomozygous108636942
1265291873265291874TA17GENIChomozygous108636943
1265293507265293508CT26GENIChomozygous108636944
1265294538265294539CA24GENICpossibly homozygous108636945
1265296127265296128AG19GENIChomozygous108636947
1265297262265297263TC21GENIChomozygous108636948