chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108235932108235933T-10GENIChomozygous51595324
10108238451108238452CT7GENICpossibly homozygous51595326
10108240909108240910AG14GENIChomozygous51595337
10108241604108241605TC16GENIChomozygous51595339
10108246885108246886AC9GENICpossibly homozygous51595343
10108248059108248060CT13GENICheterozygous51595345
10108249366108249367AG12GENIChomozygous51595347
10108249539108249540CA16GENICpossibly homozygous51595350
10108250641108250642CG9GENICheterozygous51595352