chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143455563234555633TC33GENIChomozygous113419762
143455567634555677CT33GENIChomozygous113419763
143455575334555754CT40GENIChomozygous113419764
143455592934555930AC40GENIChomozygous113419765
143455646634556467AT49GENIChomozygous113419766
143455708034557081CT50GENIChomozygous113419767
143455778034557781TC46GENIChomozygous113419768
143455814834558149GA43GENIChomozygous113419769
143455828134558282TC41GENIChomozygous113419770
143455858934558590CT54GENIChomozygous113419771
143455912534559126GA30GENIChomozygous113419772
143455925734559258TG37GENIChomozygous113419773
143455989034559891CT37GENIChomozygous113419774
143455989134559892TG37GENIChomozygous113419775
143456224934562250GA25GENIChomozygous113419776
143456233234562333AG30GENIChomozygous113419777
143456775734567758GA35GENICpossibly homozygous113419778
143456854734568548TC32GENIChomozygous113419779
143456880334568804CG20GENIChomozygous113419780
143456911134569112AG26GENIChomozygous113419781
143457041734570418CT62GENICpossibly homozygous113419782