chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121749026617490267TC26GENIChomozygous115273975
121749128217491283AG19GENIChomozygous115273979
121749138917491390CG16GENIChomozygous115273981
121749200717492008GA21GENIChomozygous115365159
121750233017502331TC16GENIChomozygous115274021
121750328917503290CT33GENIChomozygous115365160
121750480917504810GA34GENIChomozygous115365161
121750534817505349TC26GENIChomozygous115274041
121750543117505432CT26GENIChomozygous115274043
121750817117508172GA27GENIChomozygous115365162
121750994617509947AG30GENIChomozygous115365163
121751102917511030TG17GENIChomozygous115421357
121751240817512409GA19GENIChomozygous115365164
121751254017512541TG21GENIChomozygous115365165
121751259117512592CT29GENIChomozygous115365166
121751411017514111GA29GENIChomozygous115365167
121751443217514433TC30GENIChomozygous115365168
121751459417514595GC39GENIChomozygous115365169
121751607317516074CT39GENIChomozygous115365170
121751618817516189AG25GENIChomozygous115365171
121751620617516207TC24GENIChomozygous115274051
121751633417516335GA24GENIChomozygous115365172
121751682417516825AG30GENIChomozygous115365173
121751880917518810CT30GENIChomozygous115365176
121751970617519707GA28GENIChomozygous115365177
121752494617524947AG32GENIChomozygous115274059
121752632817526329TC20GENIChomozygous115274063
121752760017527601CT28GENIChomozygous115274065
121752814317528144CT25GENIChomozygous115274067
121752833917528340TA33GENIChomozygous115274069
121753043517530436AG23GENIChomozygous115274073
121753052017530521CT29GENIChomozygous115274075
121753150217531503AG39GENIChomozygous115274079
121753173417531735AG14GENIChomozygous115274081
121753220417532205GA34GENIChomozygous115274085
121753254417532545TG23GENIChomozygous115274087