chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182503996625039967TA30GENIChomozygous110309751
182504124725041248AG27GENIChomozygous110309753
182504144725041448GA19GENIChomozygous110309755
182504244325042444CT28GENIChomozygous110309757
182504323825043239TC27GENIChomozygous110309759
182504480625044807TG31GENIChomozygous110309761
182504621125046212GA29GENIChomozygous110309763
182504623125046232CT30GENIChomozygous110309765
182504877925048780CT17GENIChomozygous110309769
182504888125048882TA23GENIChomozygous110309771
182504903925049040AG39GENIChomozygous110309773
182505077425050775TC22GENIChomozygous110309775
182505355325053554TA44GENIChomozygous110309779
182505730925057310GA25GENIChomozygous110309780
182505793725057938CT37GENIChomozygous110309781
182506089825060899TC18GENIChomozygous110309782
182506372725063728CT21GENIChomozygous110309783
182506389025063891GA26GENIChomozygous110309784
182506407125064072GT19GENIChomozygous110309785
182506428125064282CA37GENIChomozygous110309786