chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4203494296203494297GA9GENICpossibly homozygous57360646
4203494370203494371AG15GENICpossibly homozygous57360648
4203494397203494398GA17GENIChomozygous57360650
4203495229203495230GA6GENIChomozygous57360652
4203495265203495266CA11GENICpossibly homozygous57360654
4203495396203495397AG11GENIChomozygous57360656
4203495522203495523TC10GENICpossibly homozygous57054115
4203495942203495943CA16GENICpossibly homozygous57360658