chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45671203456712034CCTAAGACAGGT48GENIChomozygous131352304
45671227856712279CT61GENIChomozygous113273724
45671285656712857TC40GENIChomozygous113273725
45671509556715096AT46GENIChomozygous113273726
45671511456715115TC43GENIChomozygous113273727
45672230856722312CAAT53GENIChomozygous131352305
45672868956728690GA51GENIChomozygous113273728
45672869056728691CT51GENIChomozygous113273729
45672900956729010AT67GENIChomozygous113273730
45672903656729037TC61GENIChomozygous113273731
45672958256729582GCTGCAAGGGATCCTAGGAGCTGTCCTCAAGGAATCAGAGAATATGCCTCTAAGTA38GENIChomozygous131352306
45673094156730942CT74GENIChomozygous113273737
45673142056731421TC72GENIChomozygous113273738
45673233956732340TG55GENIChomozygous113273739
45673328656733287GA58GENIChomozygous113273740
45673375556733756CT60GENICpossibly homozygous113273741
45673378856733789CT54GENICpossibly homozygous113273742
45673456556734566TC62GENIChomozygous113273743
45673509156735092GT71GENIChomozygous113273744
45673602756736028CT69GENIChomozygous113273745
45673694756736975CTGCCATGATGGACATGGGCGTGGTTGG55GENIChomozygous131352307
45673735056737351GA59GENIChomozygous113273746
45671782256717823AG58GENIChomozygous112657108