chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182598379825983799AG27GENIChomozygous125347130
182599078325990784CA24GENIChomozygous125347131
182599092325990924TC18GENIChomozygous110312636
182599263825992639AG7GENIChomozygous110312638
182599466625994667CG12GENIChomozygous110312641
182599506825995069GA12GENIChomozygous110312643
182599520525995206GA24GENIChomozygous110312645
182599528325995284AG19GENIChomozygous110312647
182599541825995419AG7GENIChomozygous110312649
182599542025995421CA8GENIChomozygous110312651
182599561125995612AG11GENIChomozygous110312653
182599567525995676TC19GENIChomozygous110312655
182599583325995834GA28GENIChomozygous110312657
182599597325995974AC20GENIChomozygous110312659
182599601125996012GC7GENIChomozygous110312661
182599602025996021TC6GENIChomozygous110312663
182599603225996033GA8GENIChomozygous110312665
182599657225996573GC24GENICpossibly homozygous110312667
182599674925996750AG12GENIChomozygous110312669
182599746325997464TA10GENIChomozygous110312673
182599623225996233CA9GENICheterozygous110455314