chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151110753211107533A10GENICheterozygous403907176
151110753211107533AG10GENICpossibly homozygous403907177
151110753511107536A9GENICheterozygous403371961
151110753511107536AG9GENICheterozygous403371962
151110753511107536AC9GENICpossibly homozygous403371963
151110753611107537A9GENICheterozygous403907178
151110753611107537AG9GENICheterozygous403907179
151110753611107537AC9GENICpossibly homozygous403907180