chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8133193032133193033AG12GENIChomozygous116906476
8133193280133193281GA15GENIChomozygous116730350
8133193743133193744GA22GENIChomozygous117921847
8133194482133194483TG29GENIChomozygous116906482
8133195346133195347GT14GENIChomozygous116730351
8133195396133195397CT22GENIChomozygous116730352
8133195851133195852CT19GENIChomozygous116906484
8133196195133196196GA10GENIChomozygous116730355
8133196285133196286CA13GENIChomozygous116906486
8133196535133196536AG18GENIChomozygous116906488
8133201832133201833GA21GENIChomozygous116906490
8133202191133202192GA22GENIChomozygous117150585
8133206270133206271AT19GENIChomozygous116906492
8133206276133206277TA22GENIChomozygous116906494
8133209324133209325GA25GENIChomozygous117150586
8133209581133209582CG19GENIChomozygous116906496
8133210683133210684AT24GENIChomozygous117150587
8133211130133211131GT11GENIChomozygous116906498
8133213265133213266TG27GENIChomozygous116730359
8133213517133213518AC61GENICheterozygous116730366
8133213519133213520CT61GENICheterozygous116730367
8133213531133213532TG65GENICheterozygous116730368
8133213537133213538TC68GENICheterozygous116906501
8133213576133213577GA61GENICheterozygous116730369
8133213618133213619AG50GENICheterozygous116730373
8133213579133213580CT59GENICheterozygous116730370
8133213600133213601GC56GENICheterozygous116730371
8133213607133213608AT53GENICheterozygous116730372
8133213624133213625CT53GENICheterozygous116730375
8133213626133213627AC52GENICheterozygous116730376
8133213840133213841TC71GENICheterozygous116730379
8133213853133213854AC72GENICheterozygous116730380
8133213882133213883GA78GENICheterozygous116730381
8133213891133213892CT72GENICheterozygous116730382
8133213900133213901AG74GENICheterozygous116730383
8133214258133214259GA23GENIChomozygous116906509
8133214484133214485GC19GENIChomozygous116906511