chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123617040123617041GA42GENICheterozygous115863746
7123617061123617062CG39GENICheterozygous115863748
7123617071123617072GA33GENICheterozygous115863750
7123617082123617083CT34GENICheterozygous115863752
7123617353123617354GA66GENICheterozygous115863756
7123617398123617399CT71GENICheterozygous115863758
7123617960123617961TG58GENIChomozygous115863760
7123618397123618398TC42GENIChomozygous115863762
7123618448123618449GT52GENICpossibly homozygous115863764
7123618480123618481GT64GENICpossibly homozygous115863766
7123618527123618528AG52GENIChomozygous115863768
7123618547123618548CA40GENICpossibly homozygous115863770
7123618552123618553CA36GENICpossibly homozygous115863772
7123618618123618619CT44GENIChomozygous115863774
7123618698123618699TG40GENIChomozygous115863776
7123618998123618999AG10GENIChomozygous115863778
7123619006123619007TC10GENIChomozygous115863780
7123619530123619531GA47GENICpossibly homozygous115863784
7123619925123619926GC57GENICpossibly homozygous115863786
7123620686123620687TG34GENIChomozygous115863788