chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8129660479129660480GT46GENICheterozygous52889894
8129669561129669562GC5GENICheterozygous52889914
8129669563129669564GC5GENICheterozygous52889916
8129716405129716406AG18GENICheterozygous52890245
8129717243129717244CT30GENICheterozygous52890247
8129717686129717687CT53GENICheterozygous52890248
8129717767129717768TC63GENICheterozygous52890250
8129717810129717811CT51GENICheterozygous52890252
8129717821129717822TC45GENICheterozygous52890254
8129724165129724166GA20GENICheterozygous52890331
8129724213129724215AG--15GENICheterozygous52890333
8129724217129724222TGCAT-----13GENICheterozygous52890335
8129724330129724331GA12GENICheterozygous52890336
8129724373129724374GA13GENICheterozygous52890338
8129724432129724433CT31GENICheterozygous52890339
8129724928129724929GC30GENICheterozygous52890341
8129725169129725170CA56GENICheterozygous52890343
8129725311129725312GA19GENICheterozygous52890344
8129725467129725468TC27GENICheterozygous52890346
8129744117129744118CCT66GENICheterozygous52890461
8129744117129744118CCTT66GENICheterozygous54475376
8129744401129744402GC82GENICheterozygous52890464
8129744767129744776CCAACATGA---------60GENICheterozygous52890465
8129744947129744948AG130GENICheterozygous52890467
8129745146129745147CT122GENICheterozygous52890468
8129757683129757684AG27GENICheterozygous52890644
8129773257129773258TC13GENICheterozygous52890910
8129786586129786587TC52GENICheterozygous52890968
8129791647129791648AG37GENICheterozygous52890982
8129854169129854170CG22INTERGENICheterozygous52891277
8129908368129908369GGT38INTERGENICheterozygous52891448
8129908376129908377AC42INTERGENICheterozygous52891450
8129908404129908405T-39INTERGENICheterozygous52891452