chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218370037218370038TC57GENIChomozygous108538127
1218370726218370727CT60GENIChomozygous108538128
1218370873218370874GC59GENIChomozygous108538129
1218370882218370883GA54GENIChomozygous108538130
1218371269218371270CT50GENIChomozygous108538131
1218371815218371816TC58GENIChomozygous108538132
1218371951218371952GA50GENIChomozygous108538133
1218372662218372663TC46GENICpossibly homozygous108538134
1218374583218374584AG56GENIChomozygous108538135
1218374619218374620GA55GENIChomozygous108538136