chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111694971111694972GA20GENIChomozygous812862316
8111695985111695986CT27GENIChomozygous812862317
8111696079111696080CT29GENIChomozygous812862318
8111696890111696891CT18GENIChomozygous812862319
8111697873111697874GT27GENICpossibly homozygous812862320
8111698989111698990GA13GENIChomozygous812862321
8111699238111699239GA33GENIChomozygous812862322
8111700389111700390CT21GENIChomozygous812862323
8111700490111700491TC31GENIChomozygous812862324
8111700575111700576TC32GENIChomozygous812862325
8111701225111701226TC34GENIChomozygous812862326
8111701419111701420AG27GENIChomozygous812862327
8111701475111701476AG30GENIChomozygous812862328
8111701800111701801CT23GENIChomozygous812862329
8111702381111702382AG26GENIChomozygous812862330
8111702844111702845AT7GENIChomozygous812862331
8111702865111702866CT6GENIChomozygous812862332
8111702954111702955CA26GENIChomozygous812862333
8111703036111703037GA19GENIChomozygous812862334
8111703159111703160GA21GENIChomozygous812862335
8111703220111703221GA22GENIChomozygous812862336
8111703564111703565GA36GENICpossibly homozygous812862337
8111703637111703638GC37GENIChomozygous812862338
8111703761111703762AT19GENIChomozygous812862339
8111703826111703827CT8GENIChomozygous812862340
8111704388111704389TG28GENIChomozygous812862341
8111704515111704516GA29GENIChomozygous812862342
8111704774111704775CT21GENIChomozygous812862343
8111706076111706077GC20GENIChomozygous812862344
8111706234111706235GA17GENIChomozygous812862345
8111708481111708482TC13GENIChomozygous812862346
8111709172111709173GC38GENIChomozygous812862347
8111712087111712088GC49GENICheterozygous812862348
8111712865111712866CA41GENIChomozygous812862349
8111712963111712964AG41GENIChomozygous812862350
8111713315111713316TC19GENICheterozygous812862351
8111713977111713978AG28GENIChomozygous812862352
8111713989111713990CG25GENIChomozygous812862353
8111719885111719886AG46GENIChomozygous812862354