chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136454775136454776GC8GENIChomozygous578479626
4136455016136455017CT22GENICpossibly homozygous578479627
4136455211136455212CT20GENICpossibly homozygous578479628
4136455928136455929CCG25GENIChomozygous717555371
4136461234136461235TC11GENICpossibly homozygous578479629
4136462014136462015AT9GENIChomozygous578479630
4136463389136463390CA21GENIChomozygous578479631
4136463552136463553A-2GENIChomozygous717555372
4136464504136464505AT8GENICheterozygous578479632
4136464843136464844AG12GENIChomozygous578479633
4136468054136468055TC20GENIChomozygous578479634
4136468193136468194AG15GENICpossibly homozygous578479635
4136469697136469698GT5GENIChomozygous578479636
4136470136136470149ACCCCAATTGTAT-------------2GENICheterozygous717555373
4136470415136470416CT19GENIChomozygous578479637
4136471761136471762TC12GENIChomozygous578479638
4136473286136473304GTTATATACGTTTCCCTG------------------3GENIChomozygous717555374
4136473779136473780T-11GENIChomozygous717555375
4136474109136474110AG19GENIChomozygous578479639