chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108235932108235933T-8GENIChomozygous51595324
10108238451108238452CT28GENIChomozygous51595326
10108238648108238649TG14GENIChomozygous51595328
10108238672108238673GT9GENIChomozygous51595333
10108238676108238677TTTTTTTTTG6GENICheterozygous52814097
10108240032108240033A-6GENICheterozygous52734290
10108240909108240910AG42GENIChomozygous51595337
10108241604108241605TC37GENIChomozygous51595339
10108246885108246886AC26GENIChomozygous51595343
10108248059108248060CT37GENIChomozygous51595345
10108249366108249367AG16GENIChomozygous51595347
10108249539108249540CA23GENIChomozygous51595350
10108250641108250642CG39GENIChomozygous51595352