chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108412292384122924CT48GENICpossibly homozygous116814025
108412361284123613TC41GENIChomozygous116814027
108412364084123641CA41GENIChomozygous116814029
108412433184124332AG52GENIChomozygous116814033
108412451784124518CT55GENIChomozygous116981469