chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15041476550414765T51GENICpossibly homozygous141161464
15045439850454399C5GENICheterozygous402946233
15045439850454399CG5GENICheterozygous402946234
15046631250466313GA51GENIChomozygous143764918
15045440050454401CG21GENICheterozygous141210317