chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
59226907592269076GT5GENIChomozygous641084559
59226961292269613CCG4GENIChomozygous751674278
59226974992269750AG7GENIChomozygous641084560
59226982092269821CT13GENIChomozygous641084561
59227056392270564GT6GENIChomozygous641084562
59227058392270588TTCTG-----5GENIChomozygous751674279
59227072392270724TC16GENIChomozygous641084563
59227105092271051AG8GENIChomozygous641084564
59227108992271090GA13GENIChomozygous641084565
59227132292271323TTA10GENIChomozygous751674280
59227250592272506CT31GENIChomozygous641084566
59227279092272791GT26GENICpossibly homozygous641084567
59227283892272839GT24GENIChomozygous641084568
59227291392272914AG14GENIChomozygous641084569
59227383292273833TC6GENIChomozygous641084570
59227418892274189CT13GENIChomozygous641084571
59227459892274599GA27GENICpossibly homozygous641084572
59227464592274646AC23GENIChomozygous641084573
59227492292274923AG21GENIChomozygous641084574
59227506992275070GA12GENIChomozygous641084575
59227522792275228CT11GENIChomozygous641084576
59227571492275715TG8GENIChomozygous641084577
59227602792276028GA14GENIChomozygous641084578
59227660492276605CG11GENIChomozygous641084579