chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91526940815269408GAAG14GENIChomozygous128683165
91526949915269499GG13GENIChomozygous128683166
91526960915269610G46GENIChomozygous128683167
91526973515269736AG44GENIChomozygous117267488
91526977315269774T24GENIChomozygous128683168
91527064515270650AAAAT37GENIChomozygous128683169
91527076415270765CT40GENIChomozygous117267489
91527110415271105TC32GENIChomozygous117267490
91527190415271905AG44GENIChomozygous117267491
91527221815272219AG41GENIChomozygous117267492
91527223115272232CT41GENIChomozygous117267493
91527233815272339AG39GENIChomozygous117267494
91527346015273461TC35GENIChomozygous117267496
91527359915273600CT53GENIChomozygous117267497
91527396415273965TC58GENIChomozygous117267498
91527397915273980AG57GENIChomozygous117267499
91527413415274135AC52GENIChomozygous117267500
91527444315274444TC32GENIChomozygous117267501
91527448115274482GC43GENIChomozygous117267502
91527458715274588GA50GENIChomozygous117267503
91527486815274869TC42GENIChomozygous117267504