chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123617040123617041GA32GENICheterozygous115863746
7123617071123617072GA24GENICpossibly homozygous115863750
7123617335123617336GC47GENICpossibly homozygous116082484
7123617353123617354GA47GENICpossibly homozygous115863756
7123617398123617399CT42GENICheterozygous115863758
7123617980123617981CT5GENIChomozygous116082485
7123618547123618548CA46GENIChomozygous115863770
7123618552123618553CA45GENIChomozygous115863772
7123618618123618619CT35GENIChomozygous115863774
7123618698123618699TG38GENIChomozygous115863776
7123619925123619926GC20GENIChomozygous115863786
7123620686123620687TG30GENIChomozygous115863788