chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17911292379112924CA18GENICheterozygous62082973
17911307579113076GA15GENICheterozygous62082974
17911349679113497CG19GENIChomozygous61443567
17911360879113609TC24GENICheterozygous61443568
17911512979115130CT13GENICheterozygous61443569
17911538979115390TA17GENIChomozygous61443570
17911563179115632AG7GENIChomozygous61443571
17911617879116179CT22GENICheterozygous61443572
17911640279116403GA18GENICheterozygous61443573
17911648979116490GGATGATT9GENIChomozygous62082976
17911706579117066AT20GENICheterozygous62082977
17911783679117837GA10GENIChomozygous61443577
17911785279117853TC10GENIChomozygous61443578
17911881379118814C-14GENIChomozygous61443579
17911955779119558GGGAAAA15GENIChomozygous61443580
17912004379120044CT16GENICheterozygous61443581
17912067879120679CT12GENICheterozygous61443582
17912109579121096TC17GENIChomozygous61443583
17912141479121415TC14GENIChomozygous61443584
17912143379121434AG14GENIChomozygous61443585
17912162279121623CT25GENIChomozygous61443586
17912180679121807CCGT8GENICheterozygous61443591
17912195779121958GA15GENICheterozygous62082980
17912252579122527AA--13GENIChomozygous61443592
17912305479123055TG12GENICheterozygous62082981
17912333079123331AG8GENIChomozygous61443594
17912416779124168GA19GENIChomozygous61443596
17912434279124343CT10GENIChomozygous61443599
17912522579125226CT6GENICheterozygous61880097
17912546479125465TC14GENIChomozygous61443601
17912567179125672TC10GENIChomozygous61443602
17912704779127048AG18GENIChomozygous61443603
17912718779127188A-12GENICheterozygous61443604
17912779079127791GT24GENIChomozygous61443605
17912853279128533AC17GENICheterozygous61880099
17912854679128547CT16GENICheterozygous61880100
17912921879129219CT17GENIChomozygous61443606
17912922279129223TC18GENIChomozygous61443607
17912936479129365TG8GENIChomozygous61443608
17913036479130365GA8GENIChomozygous61443609