chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106562174865621749CT51GENIChomozygous117013636
106562853265628532C63GENIChomozygous128825584
106562199965622003TTTG32GENIChomozygous128825582
106562328065623281CT47GENIChomozygous116619042
106562938465629385TG40GENICpossibly homozygous117013637
106562939465629395G32GENICpossibly homozygous128825586
106562940465629405G35GENICheterozygous128825587
106563014665630147TG74GENICpossibly homozygous116619050
106563017865630179TC71GENIChomozygous116619052
106563023565630236CT68GENIChomozygous116619054
106563148565631486TC62GENIChomozygous116619056
106563174365631744TC63GENIChomozygous116619058
106563236165632362AG67GENIChomozygous116619062
106563277165632772AC56GENICpossibly homozygous116619064
106563295265632953GA45GENIChomozygous116619068
106563309365633094GA63GENIChomozygous116619070
106562940165629402TG37GENICheterozygous128870752
106563174165631742TC62GENIChomozygous133239009