chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121146995811469959CA26GENIChomozygous50049598
121147017211470173AG32GENIChomozygous50049600
121147021611470217AG29GENIChomozygous50049602
121147057611470577GA15GENICpossibly homozygous50049604
121147104111471042AG43GENIChomozygous50049606
121147135411471355CT16GENIChomozygous50049608