chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221542951221542952TC41GENIChomozygous108544607
1221542989221542990GC36GENICpossibly homozygous108544609
1221543168221543169CT48GENIChomozygous108544611
1221543843221543844TC39GENIChomozygous108544613
1221544691221544692TG57GENIChomozygous108544615
1221545381221545382GA36GENIChomozygous108544617
1221545705221545706GC26GENIChomozygous108544619