chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104730073247300733TC33GENIChomozygous51637879
104730082747300828CT17GENIChomozygous51637880
104730151947301520CT28GENIChomozygous51637881
104730414747304148AG22GENIChomozygous51637882
104730509447305095CT41GENIChomozygous51637883
104730578347305784T-9GENIChomozygous51637884
104730799547307996AG39GENIChomozygous51637885
104730841347308414GC23GENIChomozygous51637886
104730842847308429CA29GENIChomozygous51637887
104730890747308908AAATG33GENIChomozygous51637888
104730986447309865GGAGAGGGACAGAGGGAC7GENIChomozygous52459456
104730988947309890TG28GENIChomozygous51637890
104730998547309986GA26GENIChomozygous51637891
104731037447310375AG33GENIChomozygous51637892
104731042147310422CA30GENIChomozygous51637893
104731073447310735TC29GENIChomozygous51637894
104731089747310898AAAAG19GENIChomozygous51637895
104731123847311239CT33GENIChomozygous51637896
104731133847311358CACTCTCTCTCTCTCTCTCT--------------------8GENICpossibly homozygous52459457
104731175847311759AG33GENIChomozygous51637898
104731176247311763AG33GENIChomozygous51637899
104731179147311792GA20GENIChomozygous51637900
104731206547312066CT29GENIChomozygous51637901
104731275347312754CT31GENIChomozygous51637902
104731334147313345TTTT----18GENIChomozygous51637903
104731362747313628TTCCAACC25GENIChomozygous51637904
104731382647313827TC36GENIChomozygous51637905
104731414847314149AAGTGTGTGTGTGTGTGT8GENIChomozygous52459458
104731451147314512GA32GENIChomozygous51637906
104731472847314729CA22GENIChomozygous51637907
104731735947317360AC25GENIChomozygous51637909
104731750047317501CCA6GENICheterozygous51876623
104731750047317501CCAAAA6GENICheterozygous52459459
104731750147317502A-6GENICheterozygous51445683
104731895347318954CT26GENIChomozygous51637910
104731918447319188ATAT----26GENIChomozygous51637911
104731949147319492A-27GENIChomozygous51637912