chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243275716243275717GA22GENIChomozygous110346575
2243275968243275969GC16GENIChomozygous110346577
2243276233243276234GA42GENIChomozygous110346579
2243276519243276520AG35GENIChomozygous110346581
2243276606243276607TC26GENIChomozygous110346583
2243277083243277084CT20GENIChomozygous111032731
2243277283243277284CT24GENICpossibly homozygous111032733
2243277288243277289TA21GENICpossibly homozygous110346585
2243279582243279583TG26GENIChomozygous110346589
2243279592243279593GT30GENIChomozygous111032735