chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110989163110989164TC21GENIChomozygous111673626
3110990086110990087AG12GENICheterozygous112292564
3110992156110992157CT17GENIChomozygous111673629
3110993244110993245CT34GENICpossibly homozygous112139077
3111009744111009745AC29GENIChomozygous111673671
3111010477111010478CT32GENICpossibly homozygous112139078
3111013015111013016GA24GENICpossibly homozygous112139080
3111013448111013449AG15GENIChomozygous111673675
3111013584111013585TC26GENIChomozygous111673677