chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123617040123617041GA56GENIChomozygous115863746
7123617071123617072GA46GENIChomozygous115863750
7123617353123617354GA44GENIChomozygous115863756
7123617398123617399CT46GENIChomozygous115863758
7123617960123617961TG57GENICpossibly homozygous115863760
7123618397123618398TC46GENIChomozygous115863762
7123618448123618449GT49GENIChomozygous115863764
7123618480123618481GT44GENIChomozygous115863766
7123618527123618528AG46GENIChomozygous115863768
7123618547123618548CA47GENIChomozygous115863770
7123618552123618553CA50GENIChomozygous115863772
7123618618123618619CT50GENIChomozygous115863774
7123618698123618699TG42GENIChomozygous115863776
7123618998123618999AG20GENIChomozygous115863778
7123619006123619007TC15GENIChomozygous115863780
7123619019123619020GT15GENIChomozygous115863782
7123619023123619024GC15GENIChomozygous128562680
7123619530123619531GA45GENICpossibly homozygous115863784
7123619922123619926TCTG24GENICheterozygous131874625
7123620686123620687TG37GENIChomozygous115863788