chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2142504541142504542GA8GENIChomozygous74855735
2142505071142505072GA7GENICpossibly homozygous74855738
2142505314142505315GT15GENICheterozygous74855753
2142505949142505950CT22GENIChomozygous74855756
2142508149142508150GA33GENIChomozygous74855759
2142508222142508223GA26GENIChomozygous74855762
2142509162142509163GC9GENIChomozygous74855765
2142509278142509279TC7GENIChomozygous74855768
2142509335142509336CT5GENICheterozygous74855771
2142509531142509532GA27GENIChomozygous74855780
2142509779142509780GA18GENIChomozygous74855783
2142510087142510088CG29GENIChomozygous74855795
2142510355142510356CA18GENIChomozygous74855801
2142510178142510179TC7GENIChomozygous75621202
2142510468142510469TG9GENICheterozygous75621203