chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146068584960685850AT6GENIChomozygous48745259
146068614360686144AG22GENICpossibly homozygous48745261
146068835760688358GC23GENIChomozygous48745267
146069034260690343TC17GENIChomozygous48745271
146069246260692463TTAAA4GENIChomozygous48745273
146069444860694449GA15GENICpossibly homozygous48745275
146069528760695292AGGAA-----14GENICheterozygous49422836
146069599260695993AC12GENIChomozygous48745279
146069627460696275GT17GENIChomozygous48745281
146069813460698137AAA---2GENIChomozygous48745283
146069814860698149AT4GENIChomozygous49288751
146069819160698192CG13GENICheterozygous48745285
146070028160700282A-6GENIChomozygous48745287
146070341860703419CT24GENIChomozygous48745289
146070477260704773GC16GENICpossibly homozygous48745291
146070555960705560AG30GENICpossibly homozygous48745299
146070567360705674GA24GENIChomozygous48745301
146070869260708693TC12GENICheterozygous48745309
146070987360709874GGTT1GENIChomozygous48745313
146071067160710672AG11GENIChomozygous48745317