chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45068780350687804AG30GENIChomozygous112647808
45068799550687996TC35GENIChomozygous112647810
45068800750688008AG35GENIChomozygous112647812
45068828050688281TC22GENIChomozygous112647814
45068856550688566GA15GENIChomozygous112647816
45068895150688952GA23GENIChomozygous112647818
45068957950689580TC32GENIChomozygous112647820
45068965750689658AG30GENIChomozygous112647822
45069016550690166AT21GENIChomozygous112647824
45069020650690207AG27GENIChomozygous112647826
45069051350690514CT47GENIChomozygous112647828
45069079450690795CT21GENIChomozygous112647830
45069128950691290AG23GENIChomozygous112647832
45069243750692438GT23GENICpossibly homozygous112647834