chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169927205169927206GA58GENICpossibly homozygous108371643
1169927351169927352CA50GENIChomozygous108371645
1169927403169927404CT53GENIChomozygous108371647
1169927472169927473TC58GENIChomozygous108371649
1169927525169927526CA47GENIChomozygous108371651
1169927623169927624AT30GENIChomozygous108371653
1169927625169927626CA29GENICpossibly homozygous108371655
1169927631169927632TG30GENIChomozygous108371657
1169927638169927639TA30GENIChomozygous108371659
1169927695169927696AC29GENIChomozygous108371661
1169927718169927719AG28GENIChomozygous108371663
1169927719169927720CT27GENIChomozygous108371665
1169927771169927772GA24GENIChomozygous108371667
1169927888169927889TC24GENIChomozygous108371669
1169927976169927977CT21GENIChomozygous108371671
1169928004169928005AT24GENICpossibly homozygous108371673