chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47890606978906070TA22GENIChomozygous112739869
47890658478906585AG27GENIChomozygous112739871
47890713978907140GA13GENIChomozygous112739873
47890827378908274AT21GENIChomozygous112739875
47890905178909052CA22GENIChomozygous112739877
47890942678909427CT29GENIChomozygous112739879
47891073778910738TC15GENIChomozygous112739881
47891521978915220TC25GENICpossibly homozygous112739883
47891629878916299GT19GENIChomozygous112739885
47891705478917055AG16GENIChomozygous112739887
47891707878917079TC21GENIChomozygous112739889
47891776578917766TG12GENIChomozygous112739891
47892118578921186AG11GENIChomozygous112739893
47892137578921376CA20GENIChomozygous112739895
47892198278921983AT23GENICpossibly homozygous112739899
47891693978916939T13GENIChomozygous128052370
47891527078915271C17GENIChomozygous128052369
47891389678913897A24GENIChomozygous128052368
47891788278917883T11GENIChomozygous128052371
47892047778920480ACG23GENIChomozygous128052372
47892240878922409A11GENIChomozygous128052373
47892293878922939A2GENIChomozygous128052374
47892406678924067AT13GENIChomozygous112739901
47892236978922370AG19GENICheterozygous129908922
47892237178922372CT19GENICheterozygous129908923