chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123617040123617041GA14GENIChomozygous115863746
7123617071123617072GA13GENIChomozygous115863750
7123617353123617354GA20GENIChomozygous115863756
7123617398123617399CT16GENIChomozygous115863758
7123617960123617961TG30GENIChomozygous115863760
7123618397123618398TC24GENIChomozygous115863762
7123618448123618449GT20GENIChomozygous115863764
7123618480123618481GT19GENIChomozygous115863766
7123618527123618528AG16GENIChomozygous115863768
7123618547123618548CA18GENIChomozygous115863770
7123618552123618553CA17GENIChomozygous115863772
7123618618123618619CT21GENIChomozygous115863774
7123618698123618699TG25GENIChomozygous115863776
7123618998123618999AG7GENIChomozygous115863778
7123619006123619007TC8GENIChomozygous115863780
7123619019123619020GT6GENIChomozygous115863782
7123619530123619531GA21GENICpossibly homozygous115863784
7123620686123620687TG21GENIChomozygous115863788
7123619023123619024GC4GENIChomozygous128562680