chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173345916173345917TG46GENICpossibly homozygous979143152
5173347489173347490TC47GENIChomozygous979143153
5173349421173349422TA55GENIChomozygous979143154
5173352523173352524CT81GENIChomozygous979143155
5173352692173352693AG70GENIChomozygous979143156
5173352901173352902TC56GENIChomozygous979143157
5173353643173353644CT41GENIChomozygous979143158
5173353717173353718GA56GENIChomozygous979143159