chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1196005141196005142CT15GENIChomozygous135781669
1196005431196005432CA22GENIChomozygous135781670
1196006212196006213AG27GENIChomozygous135781671
1196006912196006913TG22GENIChomozygous135781672
1196008081196008082GA22GENIChomozygous135781673
1196008384196008385CT22GENIChomozygous135781674
1196009017196009018TC24GENIChomozygous135781675
1196009419196009422GAT18GENIChomozygous135453102
1196010110196010111GA22GENIChomozygous135781676
1196010534196010535CG19GENIChomozygous135781677
1196011209196011210CT27GENIChomozygous135781678
1196011223196011224CA26GENIChomozygous135781679
1196011229196011230GA26GENIChomozygous135781680
1196011292196011293CT20GENIChomozygous135781681