chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117153339671533397GA35GENIChomozygous116050978
117153377271533773GA27GENICpossibly homozygous116354911
117153410571534106GT7GENICpossibly homozygous132162992
117153410971534110GT7GENICpossibly homozygous132162993
117153411371534114GT7GENICpossibly homozygous132162994
117153411771534118GT7GENICpossibly homozygous132162995
117153451171534512GA42GENIChomozygous116354912
117153493071534931GA40GENIChomozygous116050980
117153526371535264GT44GENIChomozygous116050982
117153635971536360GA40GENIChomozygous116050984
117153807671538077A25GENIChomozygous131480185
117153412171534122GT7GENICpossibly homozygous118225996
117153443871534438CACA37GENIChomozygous131480181
117153626871536269C35GENIChomozygous131480182
117153646371536477AGGTGTGCACCGCC38GENIChomozygous131480183
117153807471538075G25GENIChomozygous131480184
117153807971538080GT26GENIChomozygous118225997
117153810371538104AG22GENIChomozygous118225998
117153843371538434AG51GENIChomozygous116354913
117153865171538652TC38GENIChomozygous116050986
117153931571539316TC36GENIChomozygous116050988
117153963871539639TA21GENIChomozygous116354914
117153829771538298GT39GENIChomozygous115984866
117153859271538593AC42GENIChomozygous115984868
117153987871539879GA19GENICheterozygous118208161
117154110471541105TC44GENIChomozygous116050992
117154122171541222AG51GENIChomozygous116050994
117154154271541543T45GENIChomozygous131480186
117154260971542610CT34GENIChomozygous116050996
117154353871543539TC35GENIChomozygous115984872
117154382471543825AC17GENIChomozygous118225999
117154490671544907CT37GENIChomozygous116051000
117154647871546479AG47GENIChomozygous116051002
117154157971541580AG39GENIChomozygous116247702
117154255471542554ATATATATT34GENIChomozygous131480188