chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109550546495505465TG36GENICheterozygous51551533
109551199395511994TG21GENICheterozygous51937129
109551856695518567A-10GENICheterozygous51551559
109551995895519959CT16GENICheterozygous51551566
109552003695520037CT29GENICheterozygous51551569
109552004095520041CT30GENICheterozygous51551570
109552511095525111A-13GENICheterozygous51551581
109553584495535845TTTATC6GENIChomozygous51551605
109553694995536950CCGTGT19GENICheterozygous51551609
109553777795537778A-2GENIChomozygous51551611
109554532395545324CT16GENICheterozygous51551623
109554608195546082GC2GENIChomozygous51937132
109556484995564850TTA4GENIChomozygous51551660
109556485495564856TG--3GENIChomozygous51551661
109557945595579456AG23GENIChomozygous51551685
109558070695580707AG24GENICheterozygous51937138
109558681895586819T-35GENIChomozygous51551691
109558773895587739AG43GENICheterozygous51551692
109559855395598554TC18GENICheterozygous51551716
109559855795598558TC18GENICheterozygous51551717
109559856195598562TC17GENICheterozygous51551718
109560003495600035TC30GENICheterozygous51551720
109561204495612048GTGT----21GENICheterozygous51998173
109561378695613787CCAGAT17GENICheterozygous51551781
109561378795613791AGAT----17GENICheterozygous51998176
109562227295622273TG28GENICheterozygous51551799
109562228095622281TG27GENICheterozygous51551800
109562854995628550AAG39GENIChomozygous51551808
109563647395636474T-12GENICheterozygous51551812
109564033795640338TTTCTC18GENICheterozygous51551816
109558761495587615TA40GENICheterozygous51750811
109556497195564973TG--13GENICheterozygous52168095