chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141294283912942840TA8GENIChomozygous113347704
141294285812942859CG7GENIChomozygous113347706
141294318312943184AG10GENIChomozygous113347708
141294329112943292AT13GENIChomozygous113347710
141294370012943701CT13GENIChomozygous113347712
141294525112945252CT11GENIChomozygous113347714
141294565212945653TG10GENIChomozygous113347716
141294678712946788TC8GENIChomozygous113347718
141294782112947822GT11GENIChomozygous113347722
141294783012947831AG11GENIChomozygous113347724
141294821312948214CT6GENIChomozygous113347726
141294829012948291AG7GENIChomozygous113347729
141294855212948553TA10GENIChomozygous113347731
141294865412948655AG7GENICpossibly homozygous113574926
141294677612946777GA9GENIChomozygous113574923
141294677712946778AT9GENIChomozygous113574924
141294865212948653AG7GENICpossibly homozygous113574925
141294865612948657AG6GENICheterozygous113347735
141294865812948659AG6GENICheterozygous113574927
141294875212948753TA6GENIChomozygous113347737
141294949612949497AC13GENIChomozygous113347743
141294993112949932GA10GENIChomozygous113347745
141295046912950470GA14GENIChomozygous113347747
141295121912951220CG11GENIChomozygous113574928
141295185412951855AT14GENIChomozygous113347749
141295289912952900CT14GENIChomozygous113347751