chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5162158099162158100AG21GENICpossibly homozygous794072024
5162158644162158645CT30GENIChomozygous794072025
5162158647162158648AG25GENIChomozygous794072026
5162158648162158649CT25GENIChomozygous794072027
5162158727162158728CT45GENIChomozygous794072028
5162159839162159840GA26GENIChomozygous794072029
5162162214162162215CT28GENIChomozygous794072030
5162162883162162884AG41GENIChomozygous794072031
5162164718162164719TC27GENIChomozygous794072032