chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62620137326201374TC18GENIChomozygous947013879
62620159526201596GA28GENIChomozygous947013880
62620180226201803CA30GENIChomozygous947013881
62620202526202026CT20GENIChomozygous947013882
62620202926202030TA20GENIChomozygous947013883
62620211326202114CT21GENIChomozygous947013884
62620243526202436TA28GENIChomozygous947013885
62620257326202574CG31GENICpossibly homozygous947013886
62620283826202839AG16GENIChomozygous947013887
62620283926202840CT16GENIChomozygous947013888
62620298826202989CT20GENIChomozygous947013889
62620317526203176GT28GENIChomozygous947013890
62620317626203177AT29GENIChomozygous947013891
62620322826203229CT33GENIChomozygous947013892
62620325226203253TC33GENIChomozygous947013893
62620330126203302CT38GENIChomozygous947013894
62620425126204252TC20GENIChomozygous947013895
62620483826204839TC30GENIChomozygous947013896