chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47793455577934556GA46GENIChomozygous145472549
47793463577934636GA43GENIChomozygous141635344
47793471577934716AC31GENIChomozygous141635345
47793474977934750GT27GENIChomozygous141635346
47793479077934791GA29GENIChomozygous141635347
47793492677934927GA50GENIChomozygous141635348
47793497477934975AG50GENIChomozygous141635349
47793501577935016GC47GENIChomozygous141635350
47793509577935096CT51GENIChomozygous141635351
47793512577935126TG46GENIChomozygous141635352
47793521577935216CT56GENIChomozygous141635353
47793526677935267AG51GENIChomozygous141635354
47793586877935869GA38GENIChomozygous145472550
47793633177936332CA42GENICpossibly homozygous145472551
47793633677936337GA40GENICpossibly homozygous141635356
47793655077936551GA45GENICpossibly homozygous145472552
47793684977936850TC51GENIChomozygous141635357
47793688677936887TC45GENIChomozygous141635358
47793700377937004AG47GENIChomozygous141635359
47793700477937005TA47GENIChomozygous141635360
47793767677937677GA38GENIChomozygous145472553
47793809177938092AG48GENIChomozygous143096549
47793821977938220CG44GENIChomozygous143096550