chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1181074270181074271TC62GENIChomozygous135762639
1181074919181074920TG65GENICpossibly homozygous135762640
1181075591181075592CT58GENIChomozygous135762641
1181076628181076628G51GENIChomozygous135448830
1181077395181077397TG64GENIChomozygous135448831