chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141041132141041133CT35GENIChomozygous115939685
7141043436141043437GA24GENIChomozygous115939687
7141044243141044244GA14GENICpossibly homozygous115939688
7141049273141049274GT24GENICheterozygous115939689
7141053521141053522CG19GENIChomozygous115939690
7141054282141054283AG29GENIChomozygous115939691
7141056273141056274CT30GENIChomozygous115939692
7141060510141060511AG26GENIChomozygous115939693
7141066029141066030TC32GENIChomozygous115939695
7141066780141066781CT45GENIChomozygous115939696
7141068996141068997GA45GENIChomozygous115939697