chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121146995811469959CA14GENICpossibly homozygous50049598
121147017211470173AG19GENIChomozygous50049600
121147021611470217AG11GENIChomozygous50049602
121147104111471042AG14GENICpossibly homozygous50049606
121147135411471355CT16GENICpossibly homozygous50049608