chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804549548045496TC12GENIChomozygous67984405
84804601648046017TG20GENIChomozygous67984409
84804654748046548AG21GENIChomozygous67984414
84804690948046910AG21GENIChomozygous67984417
84804723648047237CT23GENIChomozygous67984423
84804754248047543AC24GENIChomozygous67984427
84804761148047612CT26GENIChomozygous67984431
84804798248047983TC20GENIChomozygous67984435
84804803148048032CT22GENICpossibly homozygous67984439
84804813148048132CG25GENIChomozygous67984442
84804833448048335CT32GENICpossibly homozygous67984446
84804854848048549TC31GENICpossibly homozygous67984450
84804912748049128GA22GENIChomozygous67984468
84804856348048564GA39GENICpossibly homozygous67984454
84804881048048811AC40GENIChomozygous67984457
84804893348048934AC4GENIChomozygous67984460
84804942948049430CT20GENIChomozygous67984471
84804963548049636TC18GENIChomozygous67984474
84804984748049848TC23GENIChomozygous67984477
84805013848050139TC38GENIChomozygous67984480
84805019248050193TC34GENIChomozygous67984483
84805072548050726CT18GENIChomozygous67984486
84805131848051319AC26GENIChomozygous67984490
84805202948052030TC29GENIChomozygous67984493
84805298648052987GA30GENIChomozygous67984497
84805386448053865TC27GENIChomozygous67984506
84805431848054319TC30GENIChomozygous67984509
84805433648054337CA32GENIChomozygous67984512
84805457648054577TC27GENIChomozygous67984514
84805469448054695GA18GENIChomozygous67984517
84805576248055763CA27GENIChomozygous67984519
84805581748055818CT38GENIChomozygous67984522
84805608748056088GA30GENIChomozygous67984525
84805642348056424AG29GENIChomozygous67984528
84805645148056452CA24GENIChomozygous67984531
84805693448056935GA24GENIChomozygous67984534
84805696348056964TC25GENIChomozygous67984536
84805734448057345GT20GENIChomozygous67984539