chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143455563234555633TC30GENIChomozygous113419762
143455567634555677CT22GENIChomozygous113419763
143455575334555754CT18GENIChomozygous113419764
143455592934555930AC26GENIChomozygous113419765
143455646634556467AT30GENIChomozygous113419766
143455708034557081CT23GENIChomozygous113419767
143455778034557781TC33GENIChomozygous113419768
143455814834558149GA21GENIChomozygous113419769
143455828134558282TC21GENIChomozygous113419770
143455858934558590CT24GENIChomozygous113419771
143455912534559126GA28GENIChomozygous113419772
143455925734559258TG25GENIChomozygous113419773
143455989034559891CT20GENIChomozygous113419774
143455989134559892TG20GENIChomozygous113419775
143456224934562250GA17GENIChomozygous113419776
143456233234562333AG17GENICpossibly homozygous113419777
143456775734567758GA11GENIChomozygous113419778
143456854734568548TC25GENIChomozygous113419779
143456880334568804CG22GENIChomozygous113419780
143456911134569112AG23GENIChomozygous113419781
143457041734570418CT8GENIChomozygous113419782