chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174566922045669221GC23GENICpossibly homozygous111054914
174567338445673385CT27GENIChomozygous111054916
174567379945673800AG18GENIChomozygous111054918
174567576545675766TC21GENIChomozygous111054920
174567946545679466TC23GENIChomozygous111054922