chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6101929679101929680CT27GENIChomozygous115220420
6101942691101942692GA15GENIChomozygous115220424
6101943936101943937CG16GENIChomozygous114918949
6101931160101931160T21GENIChomozygous130984962
6101935149101935150A16GENICpossibly homozygous130984963
6101947545101947546AC15GENIChomozygous115503809
6101948547101948548CT16GENICheterozygous122605948
6101948553101948554CA15GENICheterozygous122605949
6101948565101948566CA12GENICheterozygous122605950
6101948566101948567CT12GENICheterozygous122605951
6101949975101949976TG8GENICheterozygous115220426
6101950308101950309GT10GENICheterozygous115220428
6101951304101951305TG14GENIChomozygous115220430
6101951390101951391TC22GENIChomozygous115220432
6101952444101952445CT12GENIChomozygous115220434
6101961744101961745CA26GENIChomozygous115220438
6101968138101968139AG22GENIChomozygous114918970
6101974516101974517CT20GENIChomozygous114918978
6101988731101988732T13GENIChomozygous128375267
6101988848101988848TCTGATTACC22GENIChomozygous128375268
6101996334101996335C11GENICheterozygous130984964
6101996352101996353CT12GENICheterozygous115272717
6101996356101996357CT12GENICheterozygous132858646
6102000179102000180CT10GENIChomozygous115220442
6102003038102003039CT16GENIChomozygous114919050
6102003188102003189TG26GENIChomozygous115220444
6102018346102018347CT10GENICheterozygous131667806
6102018368102018369AG6GENICheterozygous131667807
6102019821102019822T13GENICheterozygous133483227
6102021287102021288CA8GENICheterozygous133167595
6102017914102017915AG10GENICheterozygous130335846
6102018119102018120GA4GENICheterozygous130335847
6102023268102023269AT13GENICheterozygous128421565
6102023909102023910TG21GENICheterozygous133743316
6102023917102023918GT23GENICheterozygous133743317
6102026417102026418CA20GENIChomozygous114919115
6102026528102026529TC23GENIChomozygous114919116
6102026858102026859AG26GENICpossibly homozygous114919117
6102026860102026860A24GENIChomozygous128375297
6102026874102026875AG29GENIChomozygous114919118