chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761639017616391CT7GENIChomozygous950796904
141761650017616501GA12GENIChomozygous950796905
141761696917616970TA30GENICpossibly homozygous950796906
141761774217617743CA18GENIChomozygous950796907
141761922817619229TA22GENIChomozygous950796908
141761998817619989GA18GENIChomozygous950796909
141762090817620909GA10GENIChomozygous950796910
141762138217621383TC22GENIChomozygous950796911
141762151417621515CT16GENIChomozygous950796912
141762219917622200CT21GENIChomozygous950796913
141762256517622566TA24GENIChomozygous950796914
141762525917625260GA28GENIChomozygous950796915
141762542117625422AC29GENIChomozygous950796916
141762588517625886AG21GENIChomozygous950796917
141762752017627521CT26GENIChomozygous950796918
141762915917629160GT23GENIChomozygous950796919
141763031317630314GA16GENIChomozygous950796920
141763041317630414CG23GENIChomozygous950796921