chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143196286143196287TC13GENIChomozygous115942944
7143196716143196717CG19GENIChomozygous116099306
7143196730143196731TC18GENIChomozygous116099308
7143197538143197539TA20GENIChomozygous116099310
7143197712143197713GA19GENIChomozygous116099312
7143197736143197737GA13GENIChomozygous118289140
7143197737143197738AC15GENIChomozygous115942945
7143197803143197804CT21GENIChomozygous116099314
7143198048143198049AC23GENIChomozygous116099316
7143198110143198111CT20GENIChomozygous116099318
7143198468143198469TC7GENIChomozygous116099320
7143198684143198685GA14GENIChomozygous116099322
7143198923143198924CT10GENICheterozygous116099324
7143199208143199209AG7GENICheterozygous116099328
7143199393143199394CG21GENIChomozygous116099330
7143199719143199720CG13GENIChomozygous116099332
7143200690143200691AG17GENIChomozygous116099334
7143201225143201226AG15GENIChomozygous116099336
7143202728143202729TC23GENIChomozygous115942946
7143203386143203387AG16GENIChomozygous115942947
7143204180143204181CA5GENIChomozygous118289142
7143204203143204204TC13GENIChomozygous116099338
7143205038143205039CT20GENIChomozygous116099356
7143205208143205209GT18GENIChomozygous116099358
7143205345143205346CT25GENIChomozygous116099360
7143205701143205702TG18GENIChomozygous116099362
7143205785143205786GC16GENIChomozygous116099364
7143205994143205995CT18GENIChomozygous116099366