chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106367635563676356TG7GENIChomozygous116616348
106368043763680438TC10GENIChomozygous116791503
106368272563682726CT7GENIChomozygous116791505
106368314263683143AG8GENIChomozygous116791507
106368459763684598GT15GENIChomozygous116791509
106368460463684605GT17GENIChomozygous116791511
106368461963684620GA15GENIChomozygous116791513
106368804863688049CT10GENIChomozygous116616362
106369009863690099GT12GENIChomozygous116791515
106369063263690633TC11GENIChomozygous116791517
106369066363690664AG13GENIChomozygous116791519
106369181763691818GA10GENIChomozygous116616366
106369215463692155AG13GENIChomozygous116791521
106369332063693321TC6GENIChomozygous116616368
106369332563693326GT5GENIChomozygous116791523
106369383263693833GT10GENIChomozygous116616370
106369446663694467GA10GENIChomozygous116791525
106369725363697254CG8GENIChomozygous116791527
106369749163697492CT12GENIChomozygous116791529
106369818263698183AG18GENIChomozygous116791531
106369850363698504TA5GENIChomozygous116791533
106369935763699358CT12GENIChomozygous116616378
106370027763700278CG7GENIChomozygous116791535
106370046363700464AG13GENIChomozygous116791537
106370108763701088TC12GENIChomozygous116791539
106370121763701218CT12GENIChomozygous116791541
106370184263701843TG12GENIChomozygous116616380
106370223063702231TG16GENIChomozygous116616384
106370278363702784CT11GENIChomozygous116616388
106370329863703299TC11GENIChomozygous116616392
106370345063703451CT18GENIChomozygous116791543
106370367863703679AG15GENIChomozygous116616396
106370499963705000GA10GENIChomozygous116791545
106370542163705422GA8GENIChomozygous116791547
106370543763705438GT11GENIChomozygous116791549
106370802163708022CA23GENIChomozygous116791551
106370856363708564AG9GENIChomozygous116616414
106370986963709870AG9GENIChomozygous116616418
106371094263710943AT5GENIChomozygous116616424
106371264163712642CT14GENIChomozygous116791553
106371921763719218CT6GENIChomozygous116791555