chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157791822157791823TC23GENIChomozygous802788779
4157791833157791834TC23GENICpossibly homozygous802788780
4157791845157791846TA24GENIChomozygous802788781
4157791851157791852TC24GENIChomozygous802788782
4157791863157791864AT22GENICpossibly homozygous802788783
4157792271157792272GA22GENIChomozygous802788784
4157793017157793018GT32GENIChomozygous802788785
4157795166157795167CT16GENICpossibly homozygous802788786
4157796662157796663TC22GENIChomozygous802788787
4157796750157796751CT30GENIChomozygous802788788
4157797124157797125GA10GENIChomozygous802788789
4157797854157797855TG18GENIChomozygous802788790
4157798356157798357TG40GENIChomozygous802788791