chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171804788218047883CT29GENIChomozygous111232809
171804817418048175TC43GENIChomozygous111232811
171804846918048470AC31GENIChomozygous111232813
171804908418049085CT35GENIChomozygous111232815
171804919318049194CT36GENIChomozygous111232817
171804935818049359GA31GENIChomozygous111232819
171804939018049391CT28GENIChomozygous111232821
171804941518049416AG26GENIChomozygous111232823
171804945918049460GA31GENIChomozygous111232825
171804958118049582CT22GENIChomozygous111232827
171804965818049659AG27GENIChomozygous111232829
171804969518049696GA26GENIChomozygous111232831
171804969818049699GA28GENIChomozygous111232833
171804974318049744TG29GENIChomozygous111232835
171804974518049746AG29GENIChomozygous111232837
171804975318049754TA24GENIChomozygous111232839
171804979818049799CT38GENIChomozygous111232841
171805057118050572CT32GENIChomozygous111232843
171805141818051419GA30GENIChomozygous111232845
171805143818051439CT35GENIChomozygous111232847
171805166518051666CA23GENIChomozygous111232849
171805253618052537TC17GENIChomozygous111232853
171805385618053857TC33GENIChomozygous111232861
171805615018056151AG21GENIChomozygous111232863
171805668818056689AT25GENIChomozygous111232865
171805715518057156CT29GENIChomozygous111232867
171805732818057329CT28GENIChomozygous111232869
171805790218057903GT27GENIChomozygous111232871
171805798318057984AG29GENIChomozygous111232873
171805818318058184GA33GENIChomozygous111232875
171805820218058203AG38GENIChomozygous111232877
171805759318057594AT28GENIChomozygous111337312
171805352818053529TA7GENIChomozygous111337310