chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216661250216661251CT21GENICpossibly homozygous61082970
1216661488216661489AG26GENIChomozygous61082971
1216661503216661504TC23GENIChomozygous61082972
1216661590216661591AG17GENIChomozygous61082973
1216661741216661742CCT12GENIChomozygous61082974
1216662166216662167CT18GENIChomozygous61082975
1216662445216662446CT22GENIChomozygous61082976
1216662682216662683CT28GENIChomozygous61082977
1216662798216662799GC20GENIChomozygous61082978
1216662844216662845CG27GENIChomozygous61082979