chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109764909597649096TC30GENICpossibly homozygous116694444
109765001697650017CT47GENIChomozygous116694446
109765107797651078CT35GENIChomozygous116694448
109765428897654289TA35GENIChomozygous116694450
109765778797657788TC29GENIChomozygous116694456
109765865897658659GA52GENIChomozygous116694458
109765967797659678TC47GENIChomozygous116694460
109766199897661999GA26GENIChomozygous116694462
109766343097663431GA43GENICheterozygous118010344
109766467597664676TA25GENIChomozygous116694464
109766513997665140TG39GENICpossibly homozygous116694466
109766573697665737AG43GENIChomozygous116694468
109766654397666544AG41GENIChomozygous116694470
109766817997668180CT33GENIChomozygous116694472
109766888397668884AG52GENIChomozygous117180971
109766890197668902AG53GENICpossibly homozygous117180972
109766909897669099GA41GENIChomozygous116694474
109766993097669931TC48GENIChomozygous116694476
109767122097671221AG40GENIChomozygous116694478
109767298097672981GA48GENIChomozygous116694480
109767387497673875GA49GENIChomozygous116694482
109767447997674480TA52GENIChomozygous116694484
109767497797674978CT39GENIChomozygous116694486
109767529297675293AG32GENIChomozygous116694488
109767611297676113AG36GENIChomozygous116694490
109767700797677008CA48GENIChomozygous116694492
109767715097677151AG55GENICpossibly homozygous116694494
109767746097677461CT60GENIChomozygous116694496
109767755997677560GA63GENIChomozygous116694498
109767818997678190CT62GENIChomozygous116694500
109767819897678199TG61GENIChomozygous116694502
109767840297678403AC55GENIChomozygous116694504
109767844697678447TA46GENIChomozygous116694506
109767845097678451GA45GENIChomozygous116694508