chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1196005141196005142CT54GENIChomozygous135781669
1196005431196005432CA53GENIChomozygous135781670
1196006212196006213AG42GENICpossibly homozygous135781671
1196006912196006913TG53GENIChomozygous135781672
1196008081196008082GA45GENICpossibly homozygous135781673
1196008384196008385CT43GENIChomozygous135781674
1196009017196009018TC58GENIChomozygous135781675
1196009419196009422GAT52GENIChomozygous135453102
1196010110196010111GA52GENIChomozygous135781676
1196010534196010535CG47GENIChomozygous135781677
1196011292196011293CT59GENIChomozygous135781681
1196011209196011210CT42GENIChomozygous135781678
1196011223196011224CA42GENIChomozygous135781679
1196011229196011230GA49GENIChomozygous135781680