chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106224228862242289TG34GENICpossibly homozygous116613566
106224246962242470CT39GENIChomozygous116613568
106224296362242964TC37GENIChomozygous116613570
106224331962243320CG28GENIChomozygous116890828
106224332962243330AG28GENIChomozygous116890830
106224375062243751AG14GENIChomozygous116613572