chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216661250216661251CT23GENICpossibly homozygous61082970
1216661488216661489AG17GENIChomozygous61082971
1216661503216661504TC15GENICpossibly homozygous61082972
1216661590216661591AG8GENIChomozygous61082973
1216661741216661742CCT1GENIChomozygous61082974
1216662166216662167CT17GENIChomozygous61082975
1216662445216662446CT24GENIChomozygous61082976
1216662682216662683CT15GENIChomozygous61082977
1216662798216662799GC27GENICpossibly homozygous61082978
1216662844216662845CG13GENICpossibly homozygous61082979