chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151240759112407592AG40GENIChomozygous112452213
151240759812407599CT40GENIChomozygous112452214
151240784012407841GC38GENIChomozygous112452215
151240952812409529TC45GENIChomozygous112452216
151240977112409772CT53GENICpossibly homozygous112452217
151240995812409959GT36GENIChomozygous112985178
151241086212410863CT29GENIChomozygous112452218
151241093912410940TC28GENIChomozygous112452219
151241149012411491TC48GENIChomozygous112452220
151241211712412118TC35GENIChomozygous112452221
151241483012414831TC21GENIChomozygous112900116
151241501612415017TA29GENIChomozygous112452222
151241600512416006GA21GENIChomozygous112452223