chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73661096136610962CA6GENIChomozygous935369766
73661136636611367TC13GENIChomozygous935369767
73661191036611911AG20GENIChomozygous935369768
73661334236613343GT24GENIChomozygous935369769
73661386536613866CT26GENIChomozygous935369770
73661486636614867TC27GENIChomozygous935369771
73661944836619449AG6GENIChomozygous935369772
73662064036620641GA22GENIChomozygous935369773
73662140836621409AG32GENIChomozygous935369774
73662144436621445CT41GENIChomozygous935369775
73662236036622361GC42GENIChomozygous935369776
73662261936622620CT23GENIChomozygous935369777
73662371936623720TC23GENIChomozygous935369778
73662431036624311TG31GENIChomozygous935369779
73662527536625276TG12GENIChomozygous935369780
73662544836625449CA29GENIChomozygous935369781
73662637036626371GT27GENIChomozygous935369782
73662757536627576GC22GENIChomozygous935369783
73663175636631757GT2GENIChomozygous935369784
73663311936633120GA29GENIChomozygous935369785
73663351636633517CT25GENIChomozygous935369786
73663383236633833TC30GENIChomozygous935369787
73663564936635650CG33GENIChomozygous935369788
73663565636635657TC33GENIChomozygous935369789
73663566936635670GA30GENIChomozygous935369790
73663597436635975CA25GENIChomozygous935369791
73663928836639289TC26GENIChomozygous935369792