chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
68687992286879923AC22GENIChomozygous114885118
68688011386880114TG30GENIChomozygous115133580
68688307486883075GT17GENIChomozygous115133581
68688596186885962AG21GENIChomozygous115133582
68688607486886075AG11GENIChomozygous115133583
68688900386889004CT27GENIChomozygous115133584
68688940086889401AC31GENIChomozygous115133585
68688949586889496TG22GENIChomozygous115133586
68688964886889649TG17GENIChomozygous114885120
68688964986889650TA17GENIChomozygous114885121
68688965486889655AT18GENIChomozygous114885122
68688966986889670TA21GENIChomozygous114885123
68689062986890630AG21GENICheterozygous115133587
68689109886891099TC32GENIChomozygous115133588
68689118886891189TA29GENIChomozygous115133589
68689189886891899TG17GENICpossibly homozygous114885124
68689276686892767CT33GENIChomozygous115133590
68689442586894426TC27GENIChomozygous115133591
68689516686895167TC22GENIChomozygous115133592
68689606786896068CT24GENIChomozygous115133593
68689857286898573GA30GENIChomozygous115133594
68689867686898677TC31GENIChomozygous115133595
68689962286899623TA24GENIChomozygous115133596
68689981586899816AG21GENIChomozygous115133597
68690107886901079AG20GENIChomozygous115133598
68690247886902479AG16GENIChomozygous115133599
68690286286902863AG23GENIChomozygous115133600
68690361886903619GT27GENIChomozygous115133601
68690459886904599CT27GENIChomozygous115133602
68690479786904798TC20GENIChomozygous114885125
68690606186906062TC31GENIChomozygous115133603
68690737586907376TC37GENIChomozygous115133604
68690798786907988AC21GENIChomozygous114885126
68690860886908609TC26GENIChomozygous115133605
68690952786909528GA32GENIChomozygous115133606
68690995786909958GC21GENIChomozygous115133607
68691069786910698CT31GENIChomozygous115133608
68691500086915001GC9GENIChomozygous115133609