chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36659398566593986CT5GENIChomozygous111596627
36659429766594298TC11GENIChomozygous111596628
36659671066596711CT32GENIChomozygous111596629
36659715766597158AG44GENIChomozygous111596630
36659827366598274AG37GENIChomozygous111596631
36659847766598478AC26GENIChomozygous111596632
36660163666601637AG30GENIChomozygous111596633
36660196666601967CT28GENIChomozygous111596634
36660759866607599TG36GENIChomozygous111596635
36660814866608149CT33GENIChomozygous111596636
36661151966611520AG23GENIChomozygous111596637
36661195066611951AG14GENICpossibly homozygous111596638
36661526466615265CT47GENIChomozygous111596640
36661533766615338TA21GENIChomozygous111596641
36661627366616274CT30GENIChomozygous111596642
36661716966617170TC14GENIChomozygous111596643
36661823666618237GA33GENIChomozygous111596644
36662034266620343TC31GENIChomozygous111596645
36662324766623248TC31GENIChomozygous111596646
36662326066623261GA30GENIChomozygous111596647
36662329566623296CT30GENIChomozygous111596648
36662417966624180TC28GENIChomozygous111596649
36662817166628172CT33GENIChomozygous111596651
36662829366628294GT40GENIChomozygous111596652
36662978766629788TC27GENIChomozygous111596653
36662980766629808GA26GENIChomozygous111596654