chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112896688428966885GA23GENIChomozygous50705024
112896698028966981CT17GENIChomozygous50705026
112896707528967076AC24GENIChomozygous50705028
112896771628967717CT26GENIChomozygous50705030
112896823228968233TC39GENIChomozygous50705032
112896944128969442AG32GENIChomozygous50705034
112897047528970476GGAGAGAGAGA2GENICheterozygous51255940
112897157328971574AG28GENIChomozygous50705036
112897293928972940TG18GENIChomozygous50705038
112897312928973130AT26GENICpossibly homozygous50705040
112897354328973544TC19GENIChomozygous50705042
112897426828974269CT31GENIChomozygous50705044
112897435128974352TC35GENIChomozygous50705046
112897452728974528TTGGTTAGAC28GENICpossibly homozygous50705048
112897467028974671AAT17GENICpossibly homozygous50705050
112897469028974693AGT---16GENICpossibly homozygous50705052
112897471928974720CT17GENICpossibly homozygous50705054