chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203426243203426244CT32GENIChomozygous110210179
2203426672203426673TC8GENIChomozygous110210181
2203426692203426693GA8GENIChomozygous120306899
2203431461203431462AG18GENIChomozygous120306900
2203431565203431566TC30GENIChomozygous110210184
2203432512203432513AT12GENIChomozygous110210185
2203441879203441880TC22GENIChomozygous120306901
2203447503203447504AG38GENIChomozygous110210189
2203450180203450181GA32GENIChomozygous120306902
2203452642203452643AC31GENIChomozygous110210192
2203452957203452958AC19GENIChomozygous110210193
2203454183203454184CT40GENIChomozygous120306903
2203455920203455921AG20GENIChomozygous120130246
2203456031203456032CT24GENIChomozygous120306904
2203456455203456456CT38GENIChomozygous120306905
2203458553203458554AG31GENIChomozygous110210202
2203458727203458728AG23GENIChomozygous110210203
2203459077203459078AG28GENIChomozygous120306906
2203460162203460163CT32GENIChomozygous120306907
2203461622203461623CA19GENIChomozygous120306908
2203463371203463372GA32GENIChomozygous120306909
2203464237203464238AG39GENIChomozygous110210213
2203464822203464823TC30GENIChomozygous110210215
2203466619203466620GA29GENIChomozygous110210217
2203467824203467825CA31GENIChomozygous110210218
2203471708203471709TC15GENIChomozygous120306910
2203473548203473549TG33GENIChomozygous110210225
2203474027203474028CA28GENIChomozygous110619512
2203490483203490484AG26GENIChomozygous110210287
2203492390203492391AT28GENIChomozygous120130248
2203492391203492392AC30GENIChomozygous120130249
2203492404203492405AG30GENIChomozygous110210293
2203492406203492407AG33GENIChomozygous110210294