chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123883010538830106CT11GENIChomozygous115324096
123883480038834801TC19GENIChomozygous115324098
123883519238835193TC15GENIChomozygous115324100
123883574438835745AG19GENIChomozygous115324102
123883605338836054AG20GENIChomozygous115324104
123883653138836532GT12GENIChomozygous115521614
123883654438836545AG11GENIChomozygous118270094
123883655638836557CT11GENIChomozygous118270095
123883688338836884CT17GENIChomozygous115324106
123883715938837160TA26GENIChomozygous115324108
123883717738837178TC25GENIChomozygous115324110
123883749538837496CT22GENIChomozygous115324112
123883761238837613GT30GENIChomozygous115324114
123883769238837693CA19GENIChomozygous115324116
123883655038836551GC11GENIChomozygous115583064
123883657138836572GA13GENIChomozygous129017089
123883657238836573AG13GENIChomozygous129017090
123883814538838146CT20GENIChomozygous115324118
123883825338838254CT10GENIChomozygous115324120
123883924938839250CT15GENIChomozygous115324122