chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121206592412065925AG9GENIChomozygous50053983
121206655112066552AT22GENICheterozygous50053989
121206655212066553AT22GENICheterozygous50053992
121206659712066598TC20GENICpossibly homozygous50053994
121206673612066737GA14GENIChomozygous50053996
121206751512067516GT3GENIChomozygous50053998