chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109620784896207849CA17GENIChomozygous118009830
109622922996229230GC24GENIChomozygous116689820
109622935696229357AC22GENIChomozygous117088929
109622939796229398TA10GENIChomozygous117297094
109623575896235759CA19GENIChomozygous118009833
109634092196340922GA14GENIChomozygous117413979
109638632096386321TC34GENIChomozygous116690488
109639246796392468GT12GENIChomozygous118009891
109641062096410621CT2GENIChomozygous117174010
109641432696414327GA13GENICheterozygous118051609
109645958996459590CT8GENICpossibly homozygous116907021
109650772296507723TG26GENIChomozygous116691067
109650605096506051CG31GENIChomozygous116827933
109651582896515829AG21GENICpossibly homozygous116956162
109652960096529601CA31GENIChomozygous118009943
109652986296529863CT23GENIChomozygous116691127
109652987396529874AC23GENIChomozygous116691129
109652998096529981GT24GENIChomozygous118009944
109653114296531143AG31GENIChomozygous117174014
109653191096531911CA22GENIChomozygous116691137
109653269396532694GA27GENIChomozygous117174016
109653804496538045GA16GENIChomozygous116827935
109655143196551432GC15GENIChomozygous116691237
109655148996551490GC18GENIChomozygous116691239
109655154096551541AC29GENICpossibly homozygous118009949