chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106621032866210329TTC9GENIChomozygous51479321
106621062066210621TG16GENIChomozygous51479322
106621084766210848CT26GENIChomozygous51479323
106621126766211268AG19GENIChomozygous51479324
106621277566212776TC28GENIChomozygous51479325
106621308266213083CCA21GENIChomozygous51479326
106621351666213517AG18GENIChomozygous51479327
106621490766214908TC28GENIChomozygous51479328