chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122556860625568607AG24GENICpossibly homozygous50141415
122556864925568650CT18GENIChomozygous50141418
122556937225569373CT19GENIChomozygous50141420
122556957925569580TC13GENICheterozygous50141422
122556977725569778CT16GENIChomozygous50141424
122557031125570312GGGGGA3GENICheterozygous50611429
122557073525570736CT14GENIChomozygous50141428
122557139125571392AG20GENIChomozygous50141430
122557184925571853AGTG----4GENICheterozygous50141432
122557200725572008GA12GENICpossibly homozygous50141434
122557255125572552GA16GENIChomozygous50141440
122557261525572616TTC3GENIChomozygous50141444
122557276325572764AG17GENIChomozygous50141448
122557287725572878AG13GENIChomozygous50141450
122557355125573552TC15GENICpossibly homozygous50141452
122557357625573577GC21GENIChomozygous50141454
122557361225573613AG18GENICpossibly homozygous50141456
122557371925573720TC13GENIChomozygous50141458
122557382625573827AT13GENICheterozygous50141460
122557418325574184GA9GENICheterozygous50141462
122557437625574377AC8GENIChomozygous50141464
122557437925574380CT6GENIChomozygous50141466
122557445325574454AC15GENICpossibly homozygous50141468