chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221248982221248983GA28GENIChomozygous108544111
1221249177221249178CT35GENIChomozygous108544113
1221249222221249223CT42GENIChomozygous108544117
1221249340221249341CA35GENIChomozygous108544119
1221249597221249598TG39GENIChomozygous108544121
1221250335221250336GA33GENIChomozygous108544123
1221250759221250760CG32GENIChomozygous108544125
1221250780221250781CT34GENIChomozygous108544127
1221250833221250834AG39GENIChomozygous108544129
1221250881221250882GA28GENIChomozygous108544131
1221251486221251487CG17GENIChomozygous108544143
1221251573221251574CA14GENICpossibly homozygous108544145
1221251944221251945CT23GENIChomozygous108544147
1221252182221252183TC28GENIChomozygous108544149