chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804549548045496TC5GENIChomozygous67984405
84804601648046017TG15GENIChomozygous67984409
84804654748046548AG35GENIChomozygous67984414
84804690948046910AG19GENIChomozygous67984417
84804723648047237CT24GENIChomozygous67984423
84804754248047543AC25GENICpossibly homozygous67984427
84804761148047612CT20GENIChomozygous67984431
84804798248047983TC18GENIChomozygous67984435
84804803148048032CT16GENICpossibly homozygous67984439
84804813148048132CG21GENIChomozygous67984442
84804833448048335CT9GENIChomozygous67984446
84804854848048549TC19GENIChomozygous67984450
84804856348048564GA16GENIChomozygous67984454
84804881048048811AC19GENIChomozygous67984457
84804893348048934AC8GENIChomozygous67984460
84804912748049128GA11GENIChomozygous67984468
84804942948049430CT16GENIChomozygous67984471
84804963548049636TC23GENIChomozygous67984474
84804984748049848TC17GENIChomozygous67984477
84805013848050139TC17GENIChomozygous67984480
84805019248050193TC19GENIChomozygous67984483
84805072548050726CT21GENIChomozygous67984486
84805131848051319AC17GENIChomozygous67984490
84805202948052030TC15GENIChomozygous67984493
84805298648052987GA22GENIChomozygous67984497
84805329248053293TA11GENIChomozygous67984500
84805329348053294TC12GENIChomozygous67984503
84805386448053865TC23GENIChomozygous67984506
84805431848054319TC14GENIChomozygous67984509
84805433648054337CA15GENIChomozygous67984512
84805457648054577TC32GENIChomozygous67984514
84805469448054695GA18GENIChomozygous67984517
84805576248055763CA24GENIChomozygous67984519
84805581748055818CT18GENIChomozygous67984522
84805608748056088GA26GENIChomozygous67984525
84805642348056424AG12GENIChomozygous67984528
84805645148056452CA18GENICpossibly homozygous67984531
84805693448056935GA18GENIChomozygous67984534
84805696348056964TC14GENIChomozygous67984536
84805734448057345GT13GENIChomozygous67984539