chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134920721134920722GT26GENIChomozygous114017452
5134921452134921453AT17GENICpossibly homozygous114017453
5134923981134923982AG32GENIChomozygous114017455
5134924755134924756CT20GENIChomozygous114017456
5134925066134925067TC28GENIChomozygous114017457