chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111697873111697874GT19GENIChomozygous803735955
8111698989111698990GA11GENIChomozygous803735956
8111700490111700491TC22GENIChomozygous803735957
8111700575111700576TC24GENIChomozygous803735958
8111702284111702285GA27GENIChomozygous803735959
8111706168111706169GA20GENIChomozygous803735960
8111706234111706235GA19GENIChomozygous803735961
8111706261111706262GA16GENIChomozygous803735962
8111706952111706953CT11GENIChomozygous803735963
8111708179111708180GA22GENIChomozygous803735964
8111708481111708482TC21GENIChomozygous803735965
8111709172111709173GC32GENIChomozygous803735966
8111709376111709377GA25GENIChomozygous803735967
8111710507111710508AT18GENIChomozygous803735968
8111711762111711763GT18GENIChomozygous803735969
8111713315111713316TC25GENICpossibly homozygous803735970
8111713977111713978AG28GENIChomozygous803735971
8111714595111714596AG23GENIChomozygous803735972
8111716278111716279TG21GENIChomozygous803735973
8111717640111717641GA21GENICpossibly homozygous803735974
8111718542111718543GA12GENIChomozygous803735975
8111719885111719886AG23GENIChomozygous803735976
8111720114111720115GA24GENIChomozygous803735977
8111720827111720828CT12GENIChomozygous803735978
8111720979111720980TC27GENIChomozygous803735979