chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110992350110992351CT16GENICheterozygous116873590
8110994805110994806TA58GENIChomozygous116646196
8110995560110995561AT54GENICpossibly homozygous116646198
8110996080110996081AG34GENIChomozygous116646200
8110996416110996417CT43GENIChomozygous116646202
8110997762110997763TC26GENIChomozygous116646204
8110997820110997821TA11GENIChomozygous116646206
8110997940110997941AG29GENIChomozygous116646208
8110998200110998201GA26GENIChomozygous116646210
8110999489110999490TC35GENIChomozygous116646214
8110999971110999972AG47GENIChomozygous116646216
8111000093111000094GA39GENIChomozygous116646218
8111000332111000333GC46GENIChomozygous116646220
8111001915111001916GT56GENIChomozygous116646222
8111002151111002152TG42GENIChomozygous116646224
8111002674111002675AC50GENICheterozygous116646226
8111002839111002840GA46GENICpossibly homozygous116646228
8111003096111003097CT29GENIChomozygous116646230
8111003113111003114CT30GENIChomozygous116646232
8111003124111003125GA29GENIChomozygous116646234
8111003309111003310CT20GENICheterozygous116646236
8111003339111003340GA16GENICheterozygous116646238
8111003431111003432AG20GENIChomozygous116646240
8111003850111003851GA25GENIChomozygous116646243
8111006417111006418TC29GENIChomozygous116646245
8111007443111007444CT40GENIChomozygous116646247
8111009282111009283AG46GENIChomozygous116646249
8111009629111009630AG31GENIChomozygous116646251
8111010740111010741CT32GENIChomozygous116646253
8111010802111010803AG33GENIChomozygous116646255
8111013510111013511AG36GENIChomozygous116646257
8111013703111013704AG34GENIChomozygous116646259
8111014192111014193AG37GENIChomozygous116646261
8111016545111016546CT34GENIChomozygous116646263
8111019047111019048CT21GENIChomozygous116646265
8111019119111019120AG26GENIChomozygous116646267
8111020140111020141TC38GENIChomozygous116646269
8111022479111022480GA40GENIChomozygous116646271