chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109707884109707885TC37GENIChomozygous116983819
10109707985109707996CGCTCGAGGAC58GENIChomozygous132148046
10109708375109708376GA44GENIChomozygous116909707
10109708616109708617AG35GENIChomozygous116909709
10109710993109710994CA38GENIChomozygous116909710
10109711454109711455AG43GENIChomozygous116719021
10109712254109712254T68GENIChomozygous132148047
10109712255109712256AC65GENIChomozygous116909711
10109712825109712825CACACACACACA21GENIChomozygous132148048
10109714734109714735TC43GENIChomozygous117072051
10109714738109714738CTGGGCTGTGGGTCAGGTTGCCCATTCTTGGCTGAATGC43GENIChomozygous132148049
10109714779109714780CT45GENIChomozygous116909712
10109715206109715207CT62GENIChomozygous116909713
10109716180109716181AT64GENICpossibly homozygous116961940