chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1505033615050337AC9INTERGENIChomozygous45095789
X1505053415050535TC4INTERGENIChomozygous45095790
X1505103315051034AG9INTERGENIChomozygous45095791
X1505274415052745TC9INTERGENIChomozygous45095792
X1505302715053028TC14INTERGENIChomozygous45095793
X1505345915053460TG7INTERGENIChomozygous45095794
X1505433715054338CT19GENICheterozygous45095796
X1505439915054400AG14GENIChomozygous45095797
X1505454415054545GA16GENICheterozygous45095798
X1505461515054616AG16GENICheterozygous45095800
X1505511415055115AG9GENIChomozygous45095802
X1505519615055197CT9GENIChomozygous45095803
X1505541015055411AG6GENICheterozygous45095805
X1505555915055560TC7GENIChomozygous45095806