chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812469263812470CT15GENIChomozygous882122723
1263813162263813163GT20GENIChomozygous882122722
1263813490263813491AT15GENIChomozygous882122721
1263814009263814010GA18GENIChomozygous882122720
1263814049263814050GA21GENIChomozygous882122719
1263814336263814337CT21GENIChomozygous882122718
1263815024263815025GA21GENIChomozygous882122717
1263815347263815348CT17GENIChomozygous882122716
1263815742263815743TC19GENIChomozygous882122715
1263817318263817319CT18GENIChomozygous882122714
1263817741263817742TC20GENIChomozygous882122713
1263818713263818714CT24GENIChomozygous882122712
1263820710263820711AG6GENIChomozygous882122711
1263820811263820812TC23GENIChomozygous882122710
1263820859263820860GA18GENIChomozygous882122709
1263823241263823242GA27GENIChomozygous882122708
1263825763263825764CA13GENIChomozygous882122707
1263826117263826118CT16GENIChomozygous882122706
1263827329263827330CT17GENICpossibly homozygous882122705
1263828500263828501GT16GENIChomozygous882122704
1263830695263830696CT17GENIChomozygous882122703
1263831720263831721GA16GENIChomozygous882122702
1263832811263832812TC25GENIChomozygous882122701
1263835276263835277GA18GENIChomozygous882122700
1263835924263835925CT9GENIChomozygous882122699
1263840397263840398CT12GENIChomozygous882122698
1263843298263843299TA16GENIChomozygous882122697