chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1215542792215542793AG34GENIChomozygous108534681
1215542905215542906CG37GENIChomozygous108534682
1215543491215543492TC37GENIChomozygous108534683
1215543716215543717GA30GENIChomozygous108534684
1215543945215543946CT28GENIChomozygous108534685
1215545998215545999AG27GENIChomozygous108534687
1215546192215546193CT25GENIChomozygous109192680
1215546400215546401GA31GENIChomozygous109192682
1215546425215546426CT29GENIChomozygous108534688
1215547036215547037GA33GENIChomozygous108534690
1215547638215547639AT45GENIChomozygous108534691
1215548272215548273GA42GENIChomozygous109192684
1215548515215548516CA40GENIChomozygous108534692
1215549233215549234TC30GENIChomozygous109192686
1215549326215549327GA29GENIChomozygous109192688
1215551615215551616CT31GENIChomozygous108991083