chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62620137326201374TC45GENIChomozygous929218729
62620159526201596GA34GENIChomozygous929218730
62620180226201803CA40GENIChomozygous929218731
62620202526202026CT32GENIChomozygous929218732
62620202926202030TA33GENIChomozygous929218733
62620243526202436TA40GENIChomozygous929218734
62620257326202574CG47GENIChomozygous929218735
62620283826202839AG39GENIChomozygous929218736
62620283926202840CT38GENIChomozygous929218737
62620317526203176GT46GENIChomozygous929218738
62620317626203177AT46GENIChomozygous929218739
62620322826203229CT44GENIChomozygous929218740
62620325226203253TC45GENIChomozygous929218741
62620330126203302CT47GENIChomozygous929218742
62620425126204252TC49GENIChomozygous929218743
62620483826204839TC49GENICpossibly homozygous929218744