chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
389835598983560CT27GENIChomozygous802330092
389843058984306TA21GENIChomozygous802330093
389844238984424AG18GENIChomozygous802330094
389850278985028AG26GENIChomozygous802330095
389855888985589GT18GENIChomozygous802330096
389860328986033GT22GENIChomozygous802330097
389877528987753AG7GENIChomozygous802330098
389877628987763GC5GENICheterozygous802330099
389880268988027CT11GENICpossibly homozygous802330100
389881418988142CT18GENICpossibly homozygous802330101
389893458989346TC13GENIChomozygous802330102
389923788992379AG27GENIChomozygous802330103
389926378992638AG40GENIChomozygous802330104
389928288992829TC36GENIChomozygous802330105
389951688995169GT19GENICpossibly homozygous802330106
389973408997341AG26GENIChomozygous802330107
389990988999099GC22GENICpossibly homozygous802330108
390007959000796GA107GENICheterozygous802330109
390038999003900GC24GENIChomozygous802330110
390047889004789AG27GENIChomozygous802330111
390051979005198CT34GENIChomozygous802330112
390056279005628GA52GENIChomozygous802330113
390065329006533TC33GENIChomozygous802330114
390095229009523TC20GENIChomozygous802330115
390096289009629TC24GENIChomozygous802330116