chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110994805110994806TA19GENIChomozygous116646196
8110995560110995561AT15GENIChomozygous116646198
8110996080110996081AG18GENIChomozygous116646200
8110996416110996417CT33GENIChomozygous116646202
8110997820110997821TA14GENIChomozygous116646206
8110997940110997941AG10GENIChomozygous116646208
8110998200110998201GA24GENIChomozygous116646210
8110999489110999490TC20GENIChomozygous116646214
8110999971110999972AG23GENIChomozygous116646216
8111000093111000094GA14GENIChomozygous116646218
8111000332111000333GC43GENIChomozygous116646220
8111001915111001916GT18GENIChomozygous116646222
8111002151111002152TG21GENIChomozygous116646224
8111002674111002675AC22GENICpossibly homozygous116646226
8111002839111002840GA36GENIChomozygous116646228
8111003096111003097CT31GENIChomozygous116646230
8111003113111003114CT25GENIChomozygous116646232
8111003124111003125GA22GENIChomozygous116646234
8111003309111003310CT41GENICheterozygous116646236
8111003339111003340GA38GENICheterozygous116646238
8111003431111003432AG32GENIChomozygous116646240
8111003850111003851GA23GENIChomozygous116646243
8111006417111006418TC33GENIChomozygous116646245
8111007443111007444CT28GENIChomozygous116646247
8111009282111009283AG39GENIChomozygous116646249
8111009629111009630AG45GENIChomozygous116646251
8111010740111010741CT30GENIChomozygous116646253
8111010802111010803AG31GENIChomozygous116646255
8111013510111013511AG34GENIChomozygous116646257
8111013703111013704AG33GENIChomozygous116646259
8111014192111014193AG34GENIChomozygous116646261
8111016545111016546CT50GENIChomozygous116646263
8111019047111019048CT30GENIChomozygous116646265
8111019119111019120AG43GENIChomozygous116646267
8111020140111020141TC32GENIChomozygous116646269
8111022479111022480GA27GENIChomozygous116646271