chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104730073247300733TC28GENIChomozygous51637879
104730082747300828CT22GENIChomozygous51637880
104730151947301520CT32GENIChomozygous51637881
104730414747304148AG36GENIChomozygous51637882
104730509447305095CT34GENIChomozygous51637883
104730578347305784T-4GENIChomozygous51637884
104730799547307996AG22GENIChomozygous51637885
104730841347308414GC27GENIChomozygous51637886
104730842847308429CA30GENIChomozygous51637887
104730890747308908AAATG33GENIChomozygous51637888
104730988947309890TG15GENIChomozygous51637890
104730998547309986GA26GENIChomozygous51637891
104731037447310375AG36GENIChomozygous51637892
104731042147310422CA27GENIChomozygous51637893
104731073447310735TC23GENIChomozygous51637894
104731089747310898AAAAG18GENIChomozygous51637895
104731123847311239CT12GENIChomozygous51637896
104731175847311759AG21GENIChomozygous51637898
104731176247311763AG21GENIChomozygous51637899
104731179147311792GA21GENIChomozygous51637900
104731206547312066CT31GENIChomozygous51637901
104731275347312754CT38GENIChomozygous51637902
104731334147313345TTTT----18GENIChomozygous51637903
104731362747313628TTCCAACC21GENIChomozygous51637904
104731382647313827TC28GENIChomozygous51637905
104731451147314512GA33GENIChomozygous51637906
104731472847314729CA30GENICpossibly homozygous51637907
104731735947317360AC19GENIChomozygous51637909
104731750047317501CCA8GENICheterozygous51876623
104731750047317501CCAAAA8GENICheterozygous52459459
104730986447309865GGAGAGGGACAGAGGGAC9GENIChomozygous52459456
104731133847311358CACTCTCTCTCTCTCTCTCT--------------------4GENICheterozygous52459457
104731414847314149AAGTGTGTGTGTGTGTGT16GENIChomozygous52459458
104731895347318954CT30GENIChomozygous51637910
104731918447319188ATAT----3GENIChomozygous51637911
104731949147319492A-8GENIChomozygous51637912