chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132592959225929593GC18GENIChomozygous958998335
132593001425930015CG19GENIChomozygous958998336
132593209825932099AG20GENICpossibly homozygous958998337
132593396825933969AG22GENIChomozygous958998338
132593470925934710GT34GENIChomozygous958998339
132593570825935709CT26GENIChomozygous958998340
132593592225935923GA19GENIChomozygous958998341
132593969025939691CT14GENIChomozygous958998342
132593998125939982CG21GENIChomozygous958998343
132594018025940181CA13GENIChomozygous958998344
132594036925940370GA16GENIChomozygous958998345
132594109525941096TC22GENIChomozygous958998346
132594119525941196CA25GENIChomozygous958998347
132594120825941209CT22GENIChomozygous958998348
132594173625941737AG17GENIChomozygous958998349
132594208425942085CT20GENIChomozygous958998350
132594308125943082GA54GENIChomozygous958998351
132594554825945549CT20GENIChomozygous958998352
132594982425949825TA26GENIChomozygous958998353