chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161725889517258895AG60GENIChomozygous142508694
161726013017260130G18GENICheterozygous142508695
161726016617260167TC27GENIChomozygous142532717
161726080017260801G50GENIChomozygous142508696
161726120817261208GCTGG35GENIChomozygous142508697
161726412517264126GA58GENIChomozygous142532718
161726423317264234AG56GENIChomozygous142532719
161726644417266445AG49GENIChomozygous142532720
161726817817268179TG47GENIChomozygous142532721
161726897917268980AG29GENIChomozygous142532722
161727122817271228G47GENIChomozygous142508698
161727122917271230AG46GENIChomozygous142532723
161727348617273486T67GENIChomozygous142508699
161727163917271640AG40GENIChomozygous139887866
161727222117272222TA64GENIChomozygous142532724
161727349017273491TC73GENIChomozygous142532725