chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142093605820936059TG11GENICpossibly homozygous967850950
142093631120936312AG16GENIChomozygous967850951
142093654320936544GA21GENIChomozygous967850952
142093785520937856TA5GENIChomozygous967850953
142094223220942233CA31GENIChomozygous967850954
142094848520948486CA15GENIChomozygous967850955
142094898520948986GC20GENIChomozygous967850956
142094898920948990TA19GENIChomozygous967850957
142094899220948993GT19GENIChomozygous967850958
142094899820948999TA19GENIChomozygous967850959
142094900620949007AT19GENIChomozygous967850960