chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183090975530909756AG33GENIChomozygous110321430
183090992230909923TC24GENIChomozygous110321432
183091024430910245GC24GENIChomozygous110532782
183091036330910364TC23GENIChomozygous110532784
183091042430910425GA20GENIChomozygous110321436
183091053030910531GA18GENIChomozygous110532786
183091078030910781TC19GENIChomozygous110321438
183091169330911694CT27GENIChomozygous110321446
183091175430911755CT23GENIChomozygous110321450
183091177730911778TC22GENIChomozygous110321452
183091181030911811CT31GENIChomozygous110321454
183091185730911858AG27GENIChomozygous110532791
183091204530912046AG25GENIChomozygous110532793
183091266330912664CT11GENIChomozygous110532797
183091291330912914CG17GENIChomozygous110532799
183091308330913084AT18GENIChomozygous110532801
183091309930913100GA19GENIChomozygous110532803
183091322930913230CA19GENIChomozygous110532805
183091342130913422TC9GENIChomozygous110532808
183091351130913512TC19GENIChomozygous110532810
183091354430913545AG21GENIChomozygous110532812
183091377930913780CA37GENIChomozygous110532816
183091386230913863GC29GENIChomozygous110532818
183091914930919150GA26GENIChomozygous110532822
183092113330921134TC23GENIChomozygous110321493
183092422330924224AG25GENIChomozygous110321505
183092450430924505TA21GENIChomozygous110532824
183092652230926523CT24GENIChomozygous110532826
183093072530930726AG14GENIChomozygous110630439
183093866830938669CT25GENIChomozygous110321529
183094223130942232CG28GENIChomozygous110321545
183094459430944595AG22GENIChomozygous110321555
183096183030961831CT18GENIChomozygous110589448
183096698630966987TC27GENIChomozygous110321581
183096750130967502AC23GENIChomozygous110321585
183096750330967504AC21GENIChomozygous110589454