chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45671203456712034CCTAAGACAGGT75GENIChomozygous131352304
45671227856712279CT75GENIChomozygous113273724
45671285656712857TC50GENIChomozygous113273725
45671509556715096AT62GENIChomozygous113273726
45671511456715115TC58GENIChomozygous113273727
45672230856722312CAAT70GENIChomozygous131352305
45672868956728690GA86GENIChomozygous113273728
45672869056728691CT86GENIChomozygous113273729
45672900956729010AT71GENIChomozygous113273730
45672903656729037TC75GENIChomozygous113273731
45672958256729582GCTGCAAGGGATCCTAGGAGCTGTCCTCAAGGAATCAGAGAATATGCCTCTAAGTA50GENIChomozygous131352306
45673094156730942CT63GENIChomozygous113273737
45673142056731421TC70GENIChomozygous113273738
45673233956732340TG74GENICpossibly homozygous113273739
45673328656733287GA76GENIChomozygous113273740
45673375556733756CT70GENIChomozygous113273741
45673378856733789CT67GENIChomozygous113273742
45673456556734566TC78GENIChomozygous113273743
45673509156735092GT69GENIChomozygous113273744
45673602756736028CT69GENIChomozygous113273745
45673694756736975CTGCCATGATGGACATGGGCGTGGTTGG57GENIChomozygous131352307
45673735056737351GA37GENIChomozygous113273746
45671782256717823AG51GENIChomozygous112657108