chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123883010538830106CT21GENIChomozygous115324096
123883480038834801TC18GENIChomozygous115324098
123883519238835193TC5GENICheterozygous115324100
123883574438835745AG22GENIChomozygous115324102
123883605338836054AG24GENIChomozygous115324104
123883688338836884CT20GENIChomozygous115324106
123883715938837160TA7GENIChomozygous115324108
123883717738837178TC8GENIChomozygous115324110
123883749538837496CT29GENIChomozygous115324112
123883761238837613GT18GENIChomozygous115324114
123883769238837693CA25GENIChomozygous115324116
123883788838837889GA12GENICheterozygous126173236
123883789038837891GA12GENICheterozygous126173237
123883814538838146CT9GENIChomozygous115324118
123883825338838254CT13GENIChomozygous115324120
123883924938839250CT20GENIChomozygous115324122