chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1505033615050337AC10INTERGENIChomozygous45095789
X1505053415050535TC13INTERGENIChomozygous45095790
X1505103315051034AG7INTERGENIChomozygous45095791
X1505274415052745TC13INTERGENIChomozygous45095792
X1505302715053028TC12INTERGENIChomozygous45095793
X1505345915053460TG14INTERGENIChomozygous45095794
X1505433715054338CT12GENICheterozygous45095796
X1505439915054400AG18GENIChomozygous45095797
X1505454415054545GA41GENICheterozygous45095798
X1505461515054616AG29GENICheterozygous45095800
X1505511415055115AG22GENIChomozygous45095802
X1505519615055197CT20GENIChomozygous45095803
X1505541015055411AG21GENICheterozygous45095805
X1505555915055560TC8GENIChomozygous45095806