chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18544464285444643TC52GENICpossibly homozygous142841984
18544466985444670AC53GENICpossibly homozygous142841985
18544477685444777GA48GENIChomozygous142841986
18544548185445482AG53GENIChomozygous142841987
18544576385445764GA29GENIChomozygous142841988
18544567285445673CT23GENICheterozygous140961891
18544567485445675GT24GENICheterozygous140961892
18544653085446531TC56GENIChomozygous142841989
18544676685446767TC24GENIChomozygous142841990
18544684985446850GA20GENIChomozygous142841991
18544712485447125TC51GENIChomozygous142841992
18544732585447326TC47GENIChomozygous142841993
18544789585447896AG64GENICpossibly homozygous142841994
18544878885448789GA49GENIChomozygous142841995
18544933885449339GT23GENIChomozygous142841996
18545079385450794CT46GENIChomozygous142841997
18545099485450995CT47GENIChomozygous142841998
18545129285451293TC48GENIChomozygous142841999
18545132185451322CT50GENIChomozygous142842000
18545171285451713GA48GENIChomozygous142842001
18545217685452177TC48GENIChomozygous142842002
18545218585452186GA44GENIChomozygous142842003
18545221185452212TG38GENIChomozygous142842004
18545239685452397GC40GENIChomozygous142842005
18545244085452441AC37GENIChomozygous142842006
18545281685452817GT44GENICpossibly homozygous142842007
18545307485453075TC40GENIChomozygous142842008
18545241085452410GGTCAGGGAACCTGAA42GENIChomozygous142790138