chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45922982659229827TC29GENIChomozygous141621267
45923341759233418CT30GENIChomozygous141621268
45923346459233465TG34GENIChomozygous141621269
45923553559235536GA29GENIChomozygous141621270
45923614459236145GC20GENIChomozygous137060834
45923668259236683A17GENIChomozygous136886594
45923734959237350TC37GENIChomozygous137060836
45924059959240600TC31GENIChomozygous137060843
45924061859240619TA32GENIChomozygous137060844
45924063159240632CT32GENIChomozygous137060845
45924075159240752AG25GENIChomozygous137060847
45924340759243408CA9GENICpossibly homozygous141621271
45924519759245198TC29GENIChomozygous137060850
45924659459246595CT20GENIChomozygous141621272
45924705359247054TC17GENIChomozygous141621273
45924109759241098C31GENIChomozygous141579405
45924411859244130CTGAGGGACAGC19GENIChomozygous141579406
45924757859247579AG18GENIChomozygous141621274
45924775959247760AG28GENIChomozygous137060852