chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71217956612179567TC47GENICpossibly homozygous115569623
71218187512181876CA31GENIChomozygous115569624
71218438212184383TC37GENIChomozygous115569625
71218477712184778GA42GENIChomozygous115569626