chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113088065030880651AG35GENIChomozygous973443911
113088115030881151CT33GENIChomozygous973443912
113088138830881389TC15GENIChomozygous973443913
113088292430882925TG15GENIChomozygous973443914
113088321630883217TC25GENIChomozygous973443915
113088448630884487AG22GENIChomozygous973443916
113088583130885832CT26GENIChomozygous973443917
113088615730886158CT27GENIChomozygous973443918
113088662930886630AG17GENIChomozygous973443919
113088679530886796TC13GENIChomozygous973443920
113088717930887180TC30GENIChomozygous973443921
113088725730887258GA25GENICpossibly homozygous973443922
113088948030889481AG33GENIChomozygous973443923
113088960030889601CT30GENIChomozygous973443924
113089283830892839TC27GENIChomozygous973443925