chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171479008714790088GT26GENIChomozygous111171005
171479012314790124TC21GENIChomozygous111171007
171479056014790561CT24GENIChomozygous111171009
171479061414790615CT31GENIChomozygous111171011
171479065914790660GT32GENIChomozygous111171013
171479112714791128AG27GENIChomozygous111171015
171479123514791236TG29GENIChomozygous111171017
171479177214791773GA33GENIChomozygous111171021
171479204014792041CA28GENIChomozygous111231622
171479215414792155TC43GENIChomozygous111171023
171479216214792163CA48GENIChomozygous111171025
171479229714792298TC37GENIChomozygous111171027
171479284814792849CT29GENIChomozygous111171029
171479335114793352AG38GENIChomozygous111171031
171479389514793896CT26GENIChomozygous111171033
171479399114793992CT23GENIChomozygous111171035
171479405814794059GA12GENIChomozygous111171037
171479418614794187AG19GENIChomozygous111171039
171479418714794188CA18GENIChomozygous111231624
171479419614794197CT17GENIChomozygous111171041
171479432314794324TC20GENIChomozygous111171043
171479468714794688AC34GENIChomozygous111171045
171479468814794689GC35GENIChomozygous111171047
171479553014795531CT25GENIChomozygous111171049
171479648114796482GA35GENIChomozygous111171051
171479838314798384AT11GENIChomozygous111171053
171479868614798687TG13GENIChomozygous111171055
171479938614799387AG42GENIChomozygous111171057
171480128114801282AG32GENIChomozygous111171059
171480165614801657TC28GENIChomozygous110966583
171479699014796991CG40GENIChomozygous110966577
171480185314801854CA30GENIChomozygous111171061