chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2200590305200590306TC19GENIChomozygous811230119
2200594720200594721GC24GENIChomozygous811230120
2200598800200598801TC19GENIChomozygous811230121
2200600163200600164CT21GENIChomozygous811230122
2200600268200600269CT20GENIChomozygous811230123
2200600342200600343CT26GENIChomozygous811230124
2200600531200600532CT19GENICpossibly homozygous811230125
2200600601200600602TC28GENIChomozygous811230126
2200601244200601245AG27GENIChomozygous811230127
2200601323200601324TC34GENIChomozygous811230128
2200601926200601927CT35GENICheterozygous811230129