chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
145961094459610945GC20GENIChomozygous48740786
145961110759611108GT27GENICheterozygous48740788
145961111159611112GT28GENICheterozygous48740790
145961137659611378AG--19GENIChomozygous48740792
145961255659612557GA12GENICpossibly homozygous48740794
145961874759618748TC24GENIChomozygous48740796