chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86775901167759012TA16GENIChomozygous53463955
86775947867759479CT5GENIChomozygous53463957
86775977567759776AG19GENIChomozygous53576491
86776094167760942GC19GENIChomozygous53576492
86776221367762214AG18GENIChomozygous53576493
86776232767762328TC17GENIChomozygous53576494
86776255767762558CT23GENIChomozygous53576495
86776278167762782TG11GENIChomozygous53576496
86776281267762813AG11GENIChomozygous53463961
86776334267763343CA13GENICpossibly homozygous53576497
86776417267764173AAC2GENIChomozygous53364248
86776472567764726AG10GENIChomozygous53576498
86776473867764739GGC11GENIChomozygous53576499
86776485567764856GT9GENIChomozygous53576500