chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221542951221542952TC48GENIChomozygous108544607
1221542989221542990GC42GENICpossibly homozygous108544609
1221543168221543169CT57GENIChomozygous108544611
1221543843221543844TC42GENIChomozygous108544613
1221544691221544692TG59GENIChomozygous108544615
1221545381221545382GA43GENIChomozygous108544617
1221545705221545706GC38GENIChomozygous108544619
1221546490221546491CT11GENIChomozygous108544621