chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36659398566593986CT25GENICpossibly homozygous111596627
36659429766594298TC22GENIChomozygous111596628
36659671066596711CT68GENIChomozygous111596629
36659715766597158AG39GENIChomozygous111596630
36659827366598274AG51GENIChomozygous111596631
36660163666601637AG47GENIChomozygous111596633
36660196666601967CT51GENIChomozygous111596634
36660759866607599TG52GENIChomozygous111596635
36660814866608149CT47GENIChomozygous111596636
36661151966611520AG30GENIChomozygous111596637
36661195066611951AG31GENICpossibly homozygous111596638
36661290966612910GA32GENICpossibly homozygous111596639
36661526466615265CT24GENIChomozygous111596640
36661533766615338TA30GENIChomozygous111596641
36662034266620343TC30GENIChomozygous111596645
36662324766623248TC54GENIChomozygous111596646
36662326066623261GA51GENIChomozygous111596647
36662329566623296CT59GENIChomozygous111596648
36662417966624180TC52GENIChomozygous111596649
36661999966620000GA39GENIChomozygous111914807
36662738166627382GA18GENICheterozygous111596650
36662817166628172CT50GENIChomozygous111596651
36662978766629788TC47GENIChomozygous111596653
36662980766629808GA43GENIChomozygous111596654