chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227941717227941718CT20GENIChomozygous61106068
1227941781227941782GA13GENIChomozygous61106069
1227945077227945078AG11GENICheterozygous61106071
1227947493227947494GT22GENICpossibly homozygous61106072
1227948645227948646A-4GENICheterozygous62036509
1227949108227949109CG11GENICheterozygous61106074
1227950241227950242TC10GENIChomozygous61106075
1227951483227951484TG14GENIChomozygous61106076
1227951937227951938AAG8GENIChomozygous61106077
1227951938227951939TA9GENIChomozygous62102965
1227952511227952512AG14GENIChomozygous61106078