chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121749026617490267TC16GENIChomozygous115273975
121749128217491283AG16GENIChomozygous115273979
121749138917491390CG21GENIChomozygous115273981
121749200717492008GA28GENIChomozygous115365159
121750233017502331TC7GENIChomozygous115274021
121750328917503290CT13GENIChomozygous115365160
121750480917504810GA12GENIChomozygous115365161
121750534817505349TC13GENIChomozygous115274041
121750543117505432CT18GENIChomozygous115274043
121750848517508486GA6GENIChomozygous115438137
121750994617509947AG20GENIChomozygous115365163
121751102917511030TG8GENIChomozygous115421357
121751240817512409GA20GENIChomozygous115365164
121751254017512541TG21GENIChomozygous115365165
121751259117512592CT10GENIChomozygous115365166
121751411017514111GA21GENIChomozygous115365167
121751443217514433TC11GENIChomozygous115365168
121751459417514595GC20GENIChomozygous115365169
121751607317516074CT16GENIChomozygous115365170
121751618817516189AG13GENIChomozygous115365171
121751620617516207TC17GENIChomozygous115274051
121751633417516335GA13GENIChomozygous115365172
121751682417516825AG16GENIChomozygous115365173
121751880917518810CT21GENIChomozygous115365176
121751915317519154CA10GENIChomozygous126262554
121751970617519707GA10GENIChomozygous115365177
121752381317523814TA8GENICheterozygous115703056
121752494617524947AG7GENIChomozygous115274059
121752760017527601CT12GENIChomozygous115274065
121752814317528144CT11GENIChomozygous115274067
121752833917528340TA18GENIChomozygous115274069
121753043517530436AG21GENIChomozygous115274073
121753052017530521CT13GENIChomozygous115274075
121753150217531503AG12GENIChomozygous115274079
121753173417531735AG12GENIChomozygous115274081
121753220417532205GA32GENIChomozygous115274085
121753254417532545TG7GENIChomozygous115274087