chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1215594763215594764TC40GENICpossibly homozygous108991178
1215594770215594771TC41GENICpossibly homozygous108991179
1215595167215595168GA29GENIChomozygous120592701
1215595959215595960GA33GENICpossibly homozygous108991181
1215599183215599184GA31GENIChomozygous108991183
1215599301215599302AG32GENIChomozygous108534741
1215600647215600648CT29GENIChomozygous108534744