chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67021687470216875CA27GENICpossibly homozygous115120567
67021737770217378TC27GENIChomozygous115120569
67021803270218033TC20GENIChomozygous115120571
67021965170219652AT19GENIChomozygous115120573
67021977470219775CT4GENIChomozygous115120575
67021995970219960GA8GENIChomozygous115120577