chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224872700224872701TC26GENICpossibly homozygous74728574
1224873307224873308CT22GENIChomozygous74728576
1224873460224873461TC19GENICpossibly homozygous74728578
1224873492224873493TA19GENIChomozygous74728580
1224874020224874021TC19GENICpossibly homozygous74728582