chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
164928227249282273TC29GENIChomozygous881569675
164928543849285439TC15GENIChomozygous881569676
164929703949297040CG31GENIChomozygous881569677
164929788049297881CG17GENIChomozygous881569678
164929849849298499CG13GENIChomozygous881569679
164930512649305127GC12GENIChomozygous881569680
164931035649310357AG15GENIChomozygous881569681
164931359349313594GA11GENIChomozygous881569682
164931646349316464TC10GENIChomozygous881569683
164931923349319234CT22GENIChomozygous881569684
164932100149321002TC27GENIChomozygous881569685
164932102849321029CT22GENIChomozygous881569686
164932286749322868GT5GENICheterozygous881569687
164932286849322869GT5GENICheterozygous881569688
164932292949322930CT22GENIChomozygous881569689
164932322249323223AT18GENIChomozygous881569690
164932330549323306CT12GENIChomozygous881569691
164932526949325270TC9GENIChomozygous881569692
164932595049325951AG11GENIChomozygous881569693
164932619749326198TC26GENIChomozygous881569694