chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1505033615050337AC11INTERGENIChomozygous45095789
X1505053415050535TC7INTERGENIChomozygous45095790
X1505103315051034AG1INTERGENIChomozygous45095791
X1505274415052745TC12INTERGENIChomozygous45095792
X1505302715053028TC11INTERGENIChomozygous45095793
X1505345915053460TG5INTERGENIChomozygous45095794
X1505433715054338CT9GENICheterozygous45095796
X1505439915054400AG14GENIChomozygous45095797
X1505454415054545GA14GENICheterozygous45095798
X1505461515054616AG8GENICpossibly homozygous45095800
X1505511415055115AG8GENIChomozygous45095802
X1505519615055197CT12GENIChomozygous45095803
X1505541015055411AG9GENIChomozygous45095805
X1505555915055560TC16GENIChomozygous45095806