chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106107773961077739C16GENIChomozygous138686530
106107816661078167GA22GENIChomozygous138801809
106107918761079188CA17GENICpossibly homozygous138801810
106108071961080719A14GENICpossibly homozygous138686531
106108358161083582TC23GENIChomozygous138801811
106108516761085168TC17GENIChomozygous138801812
106108677161086772TC21GENIChomozygous138801813
106108986861089869TG26GENIChomozygous138801814
106109042261090423T18GENIChomozygous403288172
106109040961090410TC18GENICheterozygous154643250
106109041861090419TC18GENICheterozygous154643252
106109042261090423TC18GENICheterozygous154643253
106109040961090410T18GENIChomozygous403288170
106109041861090419T18GENIChomozygous403288171
106109242261092423GC14GENIChomozygous138801815