chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264060117264060118AG47GENIChomozygous954111864
1264060439264060440AG34GENIChomozygous954111865
1264061026264061027AG29GENIChomozygous954111866
1264061283264061284GA37GENIChomozygous954111867
1264061466264061467TC30GENIChomozygous954111868
1264062068264062069CA9GENICpossibly homozygous954111869
1264062297264062298TC31GENIChomozygous954111870
1264062501264062502AG33GENIChomozygous954111871
1264062532264062533CT36GENIChomozygous954111872
1264062601264062602CT25GENIChomozygous954111873
1264062947264062948GA36GENIChomozygous954111874
1264064003264064004AG16GENIChomozygous954111875
1264064234264064235TG25GENIChomozygous954111876
1264064641264064642CT43GENIChomozygous954111877
1264064988264064989AG36GENIChomozygous954111878
1264065424264065425CA32GENIChomozygous954111879
1264065813264065814AT48GENIChomozygous954111880
1264066698264066699TC40GENIChomozygous954111881
1264066832264066833GA40GENIChomozygous954111882
1264066841264066842CT35GENIChomozygous954111883
1264067060264067061TC29GENIChomozygous954111884
1264067293264067294AG26GENIChomozygous954111885
1264069621264069622CT25GENIChomozygous954111886
1264069737264069738CT33GENIChomozygous954111887
1264069747264069748GA31GENIChomozygous954111888
1264070790264070791CT37GENIChomozygous954111889
1264071386264071387GA33GENIChomozygous954111890
1264071462264071463CA22GENIChomozygous954111891