chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
730990873099088TC39GENIChomozygous637982085
731001163100117CCTG27GENIChomozygous749700714
731001393100140GGT29GENIChomozygous749700715
731001443100145CCG29GENIChomozygous749700716
731001503100151CCG29GENIChomozygous749700717
731002053100206CCAACA23GENIChomozygous749700718
731019463101947GA20GENIChomozygous637982086
731020103102011CT21GENIChomozygous637982087
731020373102038CT22GENIChomozygous637982088
731020523102053GGAA18GENIChomozygous749700720
731030973103098AT26GENIChomozygous637982089
731048103104811G-21GENICpossibly homozygous749700721
731051303105131TC13GENIChomozygous637982090