chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671425266714253GA38GENIChomozygous116047956
116671647966716480TC30GENIChomozygous115888070
116671668466716685GA26GENIChomozygous115888072
116671730866717309TA7GENICpossibly homozygous115888074
116671760366717604GC18GENIChomozygous115888078
116671771366717714GA15GENIChomozygous116047958
116671894366718944AG21GENIChomozygous115888080
116672098466720985TA17GENIChomozygous115888082
116672232466722325CT17GENIChomozygous116047960
116672350966723510TC29GENIChomozygous115888092
116672411266724113AC16GENIChomozygous115888096
116672422866724229TC19GENIChomozygous115888098
116672543466725435TC13GENIChomozygous115888106
116672636166726362TC26GENIChomozygous115888110
116672675466726755GC37GENIChomozygous115888114
116672734666727347AG28GENIChomozygous115888116
116672886966728870AC19GENICpossibly homozygous115977397
116672908866729089AT22GENIChomozygous116047962
116672959066729591AT25GENIChomozygous116047964
116672969766729698TC13GENIChomozygous116047966
116673084166730842GA33GENIChomozygous115888120