chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91526940815269408GAAG19GENICpossibly homozygous128683165
91526949915269499GG25GENIChomozygous128683166
91526960915269610G51GENIChomozygous128683167
91526973515269736AG21GENIChomozygous117267488
91527076415270765CT52GENIChomozygous117267489
91527110415271105TC32GENIChomozygous117267490
91527190415271905AG69GENIChomozygous117267491
91527221815272219AG74GENIChomozygous117267492
91527223115272232CT70GENIChomozygous117267493
91527233815272339AG48GENIChomozygous117267494
91527346015273461TC45GENIChomozygous117267496
91526977315269774T14GENIChomozygous128683168
91527064515270650AAAAT44GENIChomozygous128683169
91527359915273600CT63GENIChomozygous117267497
91527396415273965TC69GENIChomozygous117267498
91527397915273980AG73GENIChomozygous117267499
91527413415274135AC51GENIChomozygous117267500
91527444315274444TC49GENIChomozygous117267501
91527448115274482GC44GENIChomozygous117267502
91527458715274588GA48GENIChomozygous117267503
91527486815274869TC56GENIChomozygous117267504