chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62777052827770529GA26GENIChomozygous115451080
62777163927771640CG20GENIChomozygous115451084
62777233327772334GT10GENIChomozygous115495124
62777326827773269AG11GENIChomozygous115451087
62777585427775855CT21GENIChomozygous115495126
62777625327776254GA18GENIChomozygous115451093
62777763827777639AT27GENIChomozygous115495128
62777835527778356TC32GENIChomozygous115495130
62777842427778425TG29GENIChomozygous115495132
62778342527783426GT22GENIChomozygous115495134
62778395127783952CT25GENIChomozygous115495136
62778492927784930TC29GENIChomozygous115495138
62778493027784931GA30GENIChomozygous115495140
62778659527786596TC18GENIChomozygous115451099
62778670927786710AC12GENIChomozygous115495142
62779033527790336TC43GENIChomozygous115451103
62779079527790796AG28GENIChomozygous115495144
62780022427800225CT28GENIChomozygous115495147
62780089027800891GA18GENIChomozygous115495149
62780308527803086GA24GENICpossibly homozygous115495153
62781482227814823TC19GENIChomozygous115451107
62781491427814915TC30GENIChomozygous115451109
62781535927815360AG23GENIChomozygous115451111