chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91602451316024514AC20GENIChomozygous631675325
91602484416024845CG14GENICpossibly homozygous631675326
91602788816027889TC16GENICpossibly homozygous631675327
91602857416028575TA27GENICpossibly homozygous631675328
91602949416029495AAG8GENIChomozygous745738063
91603178416031785TC19GENICpossibly homozygous631675329
91603193716031938GC2GENICheterozygous631675330
91603224216032243GA14GENIChomozygous631675331
91603403916034040CT14GENICpossibly homozygous631675332
91603583616035837GA12GENIChomozygous631675333
91604261816042619A-7GENICheterozygous745738066
91604451116044512GT13GENICpossibly homozygous631675334
91604724116047242CG16GENIChomozygous631675335
91604943816049439TA19GENIChomozygous631675336
91605004416050045A-8GENICheterozygous745738067
91605076216050766GTGG----6GENIChomozygous745738068
91605120716051208TC12GENICheterozygous631675337
91605261716052618TC11GENIChomozygous631675338
91605277516052776AG9GENIChomozygous631675339
91605317616053177CT5GENIChomozygous631675340
91605762616057627AG18GENICpossibly homozygous631675341
91605873616058737TC24GENICpossibly homozygous631675342
91605926316059264GA12GENICpossibly homozygous631675343