chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1215542792215542793AG26GENIChomozygous108534681
1215542905215542906CG22GENIChomozygous108534682
1215543491215543492TC42GENIChomozygous108534683
1215543716215543717GA50GENIChomozygous108534684
1215543945215543946CT19GENIChomozygous108534685
1215545998215545999AG30GENIChomozygous108534687
1215546192215546193CT21GENIChomozygous109192680
1215546400215546401GA30GENIChomozygous109192682
1215546425215546426CT30GENIChomozygous108534688
1215547036215547037GA38GENIChomozygous108534690
1215547638215547639AT36GENIChomozygous108534691
1215548272215548273GA32GENIChomozygous109192684
1215548515215548516CA21GENIChomozygous108534692
1215549233215549234TC32GENIChomozygous109192686
1215549326215549327GA37GENIChomozygous109192688
1215551615215551616CT41GENIChomozygous108991083