chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265031467265031468GC33GENIChomozygous109027731
1265031537265031538TC34GENIChomozygous109027732
1265031969265031970CT20GENIChomozygous109027733
1265032973265032974TC21GENIChomozygous108636820
1265033148265033149CT16GENIChomozygous109027734
1265033225265033226GA28GENIChomozygous108636821
1265035959265035960AT24GENIChomozygous108783630
1265036448265036449CG25GENIChomozygous108636825
1265036523265036524GA23GENIChomozygous109027735
1265036793265036794TA30GENIChomozygous109027736
1265038265265038266TG29GENIChomozygous108636826
1265038480265038481AG35GENIChomozygous108783631
1265039224265039225TC34GENIChomozygous108636827
1265039791265039792CA34GENIChomozygous109027737
1265043726265043727CT34GENIChomozygous120516190
1265041346265041347TC15GENIChomozygous108636831