chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1505033615050337AC15INTERGENICpossibly homozygous45095789
X1505053415050535TC11INTERGENIChomozygous45095790
X1505103315051034AG10INTERGENIChomozygous45095791
X1505274415052745TC21INTERGENIChomozygous45095792
X1505302715053028TC20INTERGENIChomozygous45095793
X1505345915053460TG21INTERGENIChomozygous45095794
X1505433715054338CT23GENICheterozygous45095796
X1505439915054400AG29GENIChomozygous45095797
X1505454415054545GA19GENICheterozygous45095798
X1505461515054616AG21GENICheterozygous45095800
X1505511415055115AG13GENIChomozygous45095802
X1505519615055197CT11GENIChomozygous45095803
X1505541015055411AG17GENICpossibly homozygous45095805
X1505555915055560TC19GENIChomozygous45095806