chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121206592412065925AG10GENICpossibly homozygous50053983
121206655112066552AT18GENICheterozygous50053989
121206655212066553AT18GENICheterozygous50053992
121206659712066598TC24GENIChomozygous50053994
121206673612066737GA25GENICpossibly homozygous50053996
121206751512067516GT3GENIChomozygous50053998