chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155710071155710072CT32GENIChomozygous112896682
4155710212155710213AG14GENIChomozygous112896684
4155711245155711246CT20GENIChomozygous112896690
4155711392155711393AG13GENIChomozygous112896692
4155711489155711490AG12GENIChomozygous112896694
4155713205155713206TG14GENIChomozygous112896696
4155714892155714893CT23GENIChomozygous112896698
4155715142155715143CG13GENIChomozygous112896700
4155715419155715420CT11GENIChomozygous112896702
4155717462155717463GA27GENIChomozygous112896704
4155718928155718929CA25GENIChomozygous112896706
4155719431155719432CT6GENIChomozygous112896708
4155719868155719869GA20GENIChomozygous112896710
4155719916155719917CG12GENIChomozygous112896712
4155720563155720564AG26GENIChomozygous112896714
4155720688155720689TC28GENIChomozygous112896716