chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
164771620447716205TG47GENIChomozygous111805915
164771718747717188GT54GENIChomozygous111805917
164771818547718186TC33GENIChomozygous111805919
164771977847719779AG73GENICpossibly homozygous111805921
164772115247721153CG55GENIChomozygous111805923
164772279247722793TC35GENICpossibly homozygous111979653
164772491247724913TC58GENIChomozygous111805925
164772527047725271TC76GENIChomozygous111805927