chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185464834954648350G52GENIChomozygous140225312
185464842554648426TC50GENIChomozygous142654699
185464843954648440CT54GENIChomozygous142654700
185464877654648777CG45GENIChomozygous140325193
185464901954649020TG60GENIChomozygous142654701
185464909154649092A54GENIChomozygous140225314
185464938654649387GA59GENIChomozygous140325194
185465037554650376CT46GENIChomozygous140325195
185465039954650400GA44GENIChomozygous140325196
185465040054650401CA44GENIChomozygous140325197
185465053454650535AG64GENIChomozygous140325198
185465072554650725A48GENIChomozygous140225315
185465084354650844TC57GENIChomozygous140325199
185465091454650915TC54GENIChomozygous142654702
185465120354651203AA46GENIChomozygous140225316
185465130354651304AG57GENIChomozygous140325202
185465130554651306CT57GENIChomozygous142654703
185465177354651774AC52GENIChomozygous140325203
185465200754652008AC49GENIChomozygous140325204
185465299054652991AG59GENIChomozygous140325206
185465559454655595GC52GENIChomozygous140325208
185466226854662269CT50GENIChomozygous142654704
185466488954664896GTGTGTG31GENICpossibly homozygous140225317
185466617254666173TC58GENIChomozygous140325213
185465034454650347AAT47GENIChomozygous142631266