chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85912314759123148CT20GENIChomozygous116511053
85912315359123154CA20GENIChomozygous116511055
85912318859123189TC24GENIChomozygous116511057
85912319359123194TC25GENIChomozygous116511059
85912352159123522AG16GENICpossibly homozygous116511061
85912387159123872TC19GENIChomozygous116511063
85912456359124564TC27GENIChomozygous116511065
85912461559124616GA28GENIChomozygous116511067
85912523859125239AG17GENIChomozygous116511069
85912797659127977TG32GENIChomozygous117184666
85912804659128047GA25GENIChomozygous117184667
85912967859129679AG3GENICheterozygous116511073
85912968259129683AG3GENICheterozygous116511075
85912968459129685AG3GENICheterozygous116511077
85912968659129687AG3GENICheterozygous116511079
85913217559132176GA31GENIChomozygous116511087
85913338759133388AG17GENIChomozygous116511089
85913366559133666TC23GENIChomozygous116511091
85913387759133878CT20GENIChomozygous117184668
85913711559137116CT18GENIChomozygous117184669
85913827359138274CT22GENIChomozygous117184670