chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1196005141196005142CT13GENIChomozygous135781669
1196005431196005432CA12GENIChomozygous135781670
1196006212196006213AG13GENIChomozygous135781671
1196006912196006913TG18GENIChomozygous135781672
1196008081196008082GA16GENIChomozygous135781673
1196008384196008385CT23GENIChomozygous135781674
1196009017196009018TC10GENIChomozygous135781675
1196009419196009422GAT13GENIChomozygous135453102
1196010110196010111GA13GENIChomozygous135781676
1196010534196010535CG15GENIChomozygous135781677
1196011209196011210CT7GENIChomozygous135781678
1196011223196011224CA9GENIChomozygous135781679
1196011229196011230GA10GENIChomozygous135781680
1196011292196011293CT14GENIChomozygous135781681