chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106953506469535065AG28GENIChomozygous116625548
106953518969535190GA22GENIChomozygous116625550
106953525069535251AG15GENIChomozygous116625552
106953599269535993GA30GENICpossibly homozygous118104511
106953616469536165GA14GENIChomozygous116625554
106953649669536497TC16GENIChomozygous116625556
106953656769536568AG33GENIChomozygous116625558
106953665969536660TC9GENIChomozygous116625560
106953666969536670TC9GENIChomozygous116625562
106953688669536887TC21GENIChomozygous116625564
106953690069536901AC21GENIChomozygous116625566
106953717869537179AG10GENIChomozygous116625568
106953595969535960TG5GENICheterozygous126385546