chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170796280170796281TG32GENIChomozygous109167116
1170796369170796370CT33GENICpossibly homozygous109167118
1170796918170796919CT38GENIChomozygous109167120
1170797198170797199CA46GENIChomozygous109167122