chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148252903482529035TC19GENIChomozygous66542717
148252981182529812CT20GENIChomozygous66542718
148253404082534041AG10GENIChomozygous66542719
148253582982535830GA11GENIChomozygous66542720
148253676282536763GA23GENIChomozygous66542721
148253895982538960AG25GENIChomozygous66542722
148254422682544227CT23GENIChomozygous66542723
148254846082548461TC33GENIChomozygous66542724
148255126982551270TA31GENIChomozygous66542725
148255468982554690AG23GENIChomozygous66542726
148255812882558129CT29GENIChomozygous66542727
148255851882558519CT44GENIChomozygous66542728
148255992382559924CG26GENIChomozygous66542729
148256141982561420AC25GENIChomozygous66542730
148256291982562920TC16GENIChomozygous66542731
148256309482563095TC16GENIChomozygous66542732
148256746582567466CA23GENIChomozygous66542734
148256763982567640GA19GENIChomozygous66542735
148255730682557307TA5GENIChomozygous66645911
148255739382557394GA14GENIChomozygous66645913
148257209982572100AC18GENIChomozygous66542736
148257278082572781AT24GENICpossibly homozygous66542737
148257379882573799GA24GENIChomozygous66542738
148257439582574396GT14GENIChomozygous66542739
148257442682574427TA9GENICpossibly homozygous66645919
148257483282574833AG25GENIChomozygous66542740
148257637282576373GA22GENIChomozygous66542741
148257944282579443GA17GENIChomozygous66542742