chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228740445228740446AG28GENICpossibly homozygous514986607
1228741329228741330AAGAGAG12GENIChomozygous686908075
1228743097228743098AC17GENICpossibly homozygous514986608
1228743108228743109AG17GENICpossibly homozygous514986609
1228743588228743589TG17GENICheterozygous514986610
1228744220228744221TC27GENIChomozygous514986611
1228746722228746723TC19GENIChomozygous514986612
1228751732228751733CCATTT6GENIChomozygous686908076
1228753035228753036CCCACA12GENIChomozygous686908077
1228753087228753089AC--16GENICheterozygous686908079
1228754285228754286CCT6GENICheterozygous686908080
1228755467228755468GGCA19GENICpossibly homozygous686908081
1228755483228755484AACACAC16GENICheterozygous686908082
1228755487228755488TTAC16GENICpossibly homozygous686908084
1228755487228755488TTACAC16GENICheterozygous686908085
1228756440228756441T-14GENICpossibly homozygous686908087
1228756522228756528GTGTGT------4GENIChomozygous686908089