chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121125418211254183CT21GENIChomozygous115415387
121125418411254185TC21GENIChomozygous115415389
121125441811254419AC23GENIChomozygous115437338
121125450811254509TC18GENIChomozygous115437339
121125551411255515CT24GENIChomozygous115437340
121125558311255584AT27GENIChomozygous115254928
121125560111255602AG26GENIChomozygous115254930
121125563411255635TC27GENIChomozygous115254932
121125599211255993AG17GENIChomozygous115254934
121125683111256832GA16GENIChomozygous115437341
121125684611256847TG22GENIChomozygous115254936
121125686711256868TC25GENIChomozygous115254938
121125687411256875AG25GENIChomozygous115254940
121125711611257117AC15GENIChomozygous115254942
121125754411257545AG19GENIChomozygous115254944
121125755011257551AG19GENIChomozygous115254946
121125852011258521GT33GENIChomozygous115445091
121125986611259867CA21GENIChomozygous115254950
121125989011259891GA28GENIChomozygous115254952
121126044311260444AG17GENIChomozygous115254956
121126095011260951AG19GENIChomozygous115437342
121126148511261486GA17GENIChomozygous115437343
121126149311261494AC19GENIChomozygous115482338
121126183611261837GA29GENICpossibly homozygous115437344
121126312711263128AT12GENIChomozygous115521329
121126344111263442CA16GENIChomozygous115437345
121126379511263796TG19GENIChomozygous115254970
121126433611264337GA11GENIChomozygous115254974
121126505211265053CA12GENIChomozygous115254980
121126534711265348AG10GENIChomozygous115254984
121126566111265662AT7GENIChomozygous115437346
121125886211258863AC11GENIChomozygous115361399