chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143455563234555633TC22GENIChomozygous113419762
143455567634555677CT19GENIChomozygous113419763
143455575334555754CT15GENIChomozygous113419764
143455592934555930AC19GENIChomozygous113419765
143455646634556467AT23GENIChomozygous113419766
143455708034557081CT22GENIChomozygous113419767
143455778034557781TC34GENIChomozygous113419768
143455814834558149GA27GENIChomozygous113419769
143455828134558282TC32GENIChomozygous113419770
143455858934558590CT24GENIChomozygous113419771
143455912534559126GA26GENIChomozygous113419772
143455925734559258TG29GENIChomozygous113419773
143455989034559891CT13GENIChomozygous113419774
143455989134559892TG13GENIChomozygous113419775
143456224934562250GA21GENIChomozygous113419776
143456233234562333AG25GENIChomozygous113419777
143456292534562926CG11GENICheterozygous113963671
143456775734567758GA18GENIChomozygous113419778
143456854734568548TC18GENIChomozygous113419779
143456880334568804CG17GENIChomozygous113419780
143456911134569112AG13GENIChomozygous113419781