chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123617040123617041GA59GENIChomozygous115863746
7123617071123617072GA55GENIChomozygous115863750
7123617353123617354GA63GENIChomozygous115863756
7123617398123617399CT59GENIChomozygous115863758
7123617960123617961TG55GENIChomozygous115863760
7123618397123618398TC47GENIChomozygous115863762
7123618448123618449GT54GENIChomozygous115863764
7123618480123618481GT57GENIChomozygous115863766
7123618527123618528AG55GENIChomozygous115863768
7123618547123618548CA50GENIChomozygous115863770
7123618552123618553CA50GENIChomozygous115863772
7123618618123618619CT44GENIChomozygous115863774
7123618698123618699TG44GENIChomozygous115863776
7123618998123618999AG12GENICpossibly homozygous115863778
7123619006123619007TC12GENICpossibly homozygous115863780
7123619019123619020GT12GENICpossibly homozygous115863782
7123619530123619531GA45GENICpossibly homozygous115863784
7123620686123620687TG63GENIChomozygous115863788
7123620116123620118TG41GENICheterozygous132657730
7123619023123619024GC12GENICpossibly homozygous128562680