chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71223128112231282CT45GENICpossibly homozygous115569676
71223322412233225AG27GENIChomozygous115569677
71223325112233252AG23GENIChomozygous115569678
71223374312233744GT21GENIChomozygous115569679
71223542712235428AG27GENIChomozygous115569680
71223666512236666AG28GENIChomozygous115569681
71223675512236756CT34GENIChomozygous115569682
71223735312237354GT29GENIChomozygous115569683