chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171479008714790088GT31GENIChomozygous111171005
171479012314790124TC29GENIChomozygous111171007
171479056014790561CT28GENIChomozygous111171009
171479061414790615CT32GENIChomozygous111171011
171479065914790660GT23GENIChomozygous111171013
171479112714791128AG23GENIChomozygous111171015
171479123514791236TG22GENIChomozygous111171017
171479170614791707AG37GENIChomozygous111171019
171479177214791773GA33GENIChomozygous111171021
171479204014792041CA34GENIChomozygous111231622
171479215414792155TC28GENIChomozygous111171023
171479216214792163CA27GENIChomozygous111171025
171479229714792298TC21GENIChomozygous111171027
171479284814792849CT27GENIChomozygous111171029
171479335114793352AG23GENIChomozygous111171031
171479389514793896CT23GENIChomozygous111171033
171479399114793992CT14GENIChomozygous111171035
171479405814794059GA4GENIChomozygous111171037
171479418614794187AG9GENIChomozygous111171039
171479418714794188CA9GENIChomozygous111231624
171479419614794197CT9GENIChomozygous111171041
171479432314794324TC12GENIChomozygous111171043
171479468714794688AC22GENIChomozygous111171045
171479468814794689GC22GENIChomozygous111171047
171479553014795531CT19GENIChomozygous111171049
171479648114796482GA25GENIChomozygous111171051
171479699014796991CG32GENIChomozygous110966577
171479838314798384AT8GENIChomozygous111171053
171479868614798687TG15GENIChomozygous111171055
171479938614799387AG36GENIChomozygous111171057
171480128114801282AG24GENIChomozygous111171059
171480165614801657TC18GENIChomozygous110966583
171480185314801854CA12GENIChomozygous111171061