chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266258851266258852GA23GENIChomozygous978060731
1266258863266258864GA23GENIChomozygous978060732
1266262051266262052TC19GENIChomozygous978060733
1266262453266262454GA41GENIChomozygous978060734
1266264337266264338TA50GENIChomozygous978060735
1266265228266265229AG19GENIChomozygous978060736
1266266414266266415GT2GENIChomozygous978060737
1266266712266266713CT38GENIChomozygous978060738
1266267954266267955TC49GENIChomozygous978060739
1266268309266268310GA38GENIChomozygous978060740
1266270325266270326AG14GENIChomozygous978060741