chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241504916241504917AG17GENIChomozygous109541708
1241506587241506588GA28GENIChomozygous109541710
1241507214241507215GA26GENIChomozygous109541712
1241508165241508166CA15GENIChomozygous109541714
1241508435241508436AG4GENIChomozygous109541715
1241509845241509846CG14GENIChomozygous109541717
1241510116241510117GC8GENIChomozygous120782107
1241510231241510232AG7GENIChomozygous120476557
1241510232241510233GA7GENIChomozygous120476558
1241510348241510349TA14GENIChomozygous109541720
1241510597241510598CA15GENIChomozygous109541722
1241510714241510715TC20GENIChomozygous109541724
1241512143241512144TC11GENIChomozygous109541725
1241512295241512296CT24GENIChomozygous109541727
1241512613241512614TC27GENIChomozygous109541729
1241513737241513738CG21GENIChomozygous109541730
1241514462241514463CT18GENIChomozygous109541732
1241518247241518248CT17GENIChomozygous109541735
1241520603241520604CT18GENIChomozygous109541737
1241521061241521062CT21GENIChomozygous109541738
1241522056241522057CG16GENIChomozygous109541742
1241522415241522416TG20GENIChomozygous109541743
1241523644241523645CA21GENIChomozygous109541745
1241525173241525174AG35GENIChomozygous109541747
1241528596241528597GA14GENIChomozygous109541752
1241529892241529893CG20GENIChomozygous109541756
1241530147241530148AG21GENIChomozygous109541758
1241538494241538495GA29GENIChomozygous108591068
1241538638241538639GA28GENIChomozygous109541761
1241538913241538914AC18GENIChomozygous109541763
1241551795241551796CG33GENIChomozygous109541765
1241551846241551847GA33GENIChomozygous109541767
1241553040241553041CT25GENIChomozygous109541768
1241553123241553124TG9GENIChomozygous109541770
1241554677241554678AG30GENIChomozygous109541771
1241555765241555766TG18GENIChomozygous109541773
1241556074241556075GA15GENIChomozygous109541775
1241557422241557423AG39GENIChomozygous109541779