chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241504916241504917AG19GENIChomozygous109541708
1241506587241506588GA26GENIChomozygous109541710
1241507214241507215GA17GENIChomozygous109541712
1241508165241508166CA16GENIChomozygous109541714
1241508435241508436AG10GENIChomozygous109541715
1241509845241509846CG22GENIChomozygous109541717
1241510075241510076TC15GENIChomozygous109541719
1241510116241510117GC13GENIChomozygous120782107
1241510231241510232AG15GENIChomozygous120476557
1241510232241510233GA15GENIChomozygous120476558
1241510348241510349TA15GENIChomozygous109541720
1241510597241510598CA24GENIChomozygous109541722
1241510714241510715TC35GENIChomozygous109541724
1241512143241512144TC35GENIChomozygous109541725
1241512295241512296CT34GENIChomozygous109541727
1241512613241512614TC23GENIChomozygous109541729
1241513737241513738CG37GENIChomozygous109541730
1241514462241514463CT31GENIChomozygous109541732
1241518247241518248CT23GENIChomozygous109541735
1241518869241518870AG12GENIChomozygous120686225
1241520603241520604CT27GENIChomozygous109541737
1241521061241521062CT17GENIChomozygous109541738
1241522056241522057CG33GENIChomozygous109541742
1241522415241522416TG24GENIChomozygous109541743
1241523644241523645CA23GENIChomozygous109541745
1241525173241525174AG25GENIChomozygous109541747
1241526476241526477TC20GENIChomozygous109541749
1241529892241529893CG16GENIChomozygous109541756
1241530147241530148AG13GENIChomozygous109541758
1241538494241538495GA28GENIChomozygous108591068
1241538638241538639GA17GENIChomozygous109541761
1241538913241538914AC30GENIChomozygous109541763
1241551795241551796CG20GENIChomozygous109541765
1241551846241551847GA31GENIChomozygous109541767
1241553040241553041CT8GENIChomozygous109541768
1241553123241553124TG12GENIChomozygous109541770
1241554677241554678AG26GENIChomozygous109541771
1241555765241555766TG12GENIChomozygous109541773
1241556074241556075GA17GENIChomozygous109541775
1241557422241557423AG21GENIChomozygous109541779