chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141114571411145715TC39GENICpossibly homozygous502188929
141114572211145723TC34GENIChomozygous504701938
141114572611145727CT36GENICheterozygous502188930
141114572611145727CCGT32GENIChomozygous684613003