chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1562282615622827CT18GENIChomozygous108369924
X1562303315623034GA19GENIChomozygous108369926
X1562362315623624TC27GENIChomozygous108369928
X1562377715623778AG17GENIChomozygous108369930
X1562661215626613CA12GENIChomozygous108369932