chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146068584960685850AT8GENIChomozygous48745259
146068614360686144AG29GENICpossibly homozygous48745261
146068672260686723TA4GENIChomozygous48745263
146068835760688358GC11GENICpossibly homozygous48745267
146069034260690343TC27GENICpossibly homozygous48745271
146069246260692463TTAAA8GENIChomozygous48745273
146069444860694449GA18GENICheterozygous48745275
146069599260695993AC11GENICheterozygous48745279
146069627460696275GT20GENICpossibly homozygous48745281
146069814860698149AT2GENICheterozygous49288751
146069819160698192CG8GENIChomozygous48745285
146070028160700282A-4GENICheterozygous48745287
146070341860703419CT18GENIChomozygous48745289
146070477260704773GC15GENICheterozygous48745291
146070555960705560AG28GENIChomozygous48745299
146070567360705674GA29GENICpossibly homozygous48745301
146070630160706302G-3GENIChomozygous48745303
146070869260708693TC16GENIChomozygous48745309
146071042260710423GGA1GENIChomozygous48745315
146071067160710672AG13GENICpossibly homozygous48745317