chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47890606978906070TA51GENIChomozygous112739869
47890658478906585AG41GENIChomozygous112739871
47890713978907140GA46GENIChomozygous112739873
47890827378908274AT29GENIChomozygous112739875
47890905178909052CA50GENIChomozygous112739877
47890942678909427CT41GENIChomozygous112739879
47891073778910738TC44GENIChomozygous112739881
47891521978915220TC49GENIChomozygous112739883
47891629878916299GT61GENIChomozygous112739885
47891705478917055AG41GENIChomozygous112739887
47891707878917079TC38GENIChomozygous112739889
47891776578917766TG34GENIChomozygous112739891
47891788278917883T34GENIChomozygous128052371
47891389678913897A50GENIChomozygous128052368
47891527078915271C62GENIChomozygous128052369
47891693978916939T52GENICpossibly homozygous128052370
47892047778920480ACG38GENIChomozygous128052372
47892118578921186AG46GENIChomozygous112739893
47892137578921376CA36GENIChomozygous112739895
47892198278921983AT37GENICpossibly homozygous112739899
47892240878922409A38GENICpossibly homozygous128052373
47892293878922939A27GENIChomozygous128052374
47892406678924067AT52GENICpossibly homozygous112739901