chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155710071155710072CT56GENICpossibly homozygous112896682
4155710212155710213AG57GENIChomozygous112896684
4155711069155711070CT39GENIChomozygous112896686
4155711078155711079CA41GENIChomozygous112896688
4155711245155711246CT42GENIChomozygous112896690
4155711392155711393AG47GENIChomozygous112896692
4155711489155711490AG48GENIChomozygous112896694
4155713205155713206TG44GENIChomozygous112896696
4155714892155714893CT39GENIChomozygous112896698
4155715142155715143CG25GENIChomozygous112896700
4155715419155715420CT41GENIChomozygous112896702
4155717462155717463GA41GENIChomozygous112896704
4155718928155718929CA41GENIChomozygous112896706
4155719390155719391AC37GENIChomozygous119282346
4155719431155719432CT38GENIChomozygous112896708
4155719868155719869GA41GENIChomozygous112896710
4155719916155719917CG39GENIChomozygous112896712
4155720563155720564AG40GENIChomozygous112896714
4155720688155720689TC37GENIChomozygous112896716
4155718142155718142TTA47GENIChomozygous128094686
4155712838155712840AT47GENIChomozygous128094685