chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
192579121625791217CT29GENICpossibly homozygous109673384
192579166625791667AG14GENIChomozygous109673386
192579510225795103AG31GENIChomozygous109673388
192579537825795379TG42GENIChomozygous109673390
192580116325801164AC4GENIChomozygous109673392