chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264676887264676888CT24GENIChomozygous108636504
1264676928264676929AG17GENIChomozygous108636505
1264677177264677178GA10GENIChomozygous108636507
1264679816264679817AG15GENIChomozygous108636508
1264681977264681978GT10GENIChomozygous108636510
1264685538264685539GA31GENIChomozygous108636511
1264687128264687129AG17GENIChomozygous108636512
1264691239264691240AC28GENIChomozygous108636513
1264693884264693885GC32GENIChomozygous108636516
1264695868264695869CT13GENIChomozygous108636517
1264696346264696347TC10GENIChomozygous108636519
1264698560264698561CT29GENIChomozygous108636523
1264698738264698739TC21GENIChomozygous108636524
1264699192264699193AG16GENIChomozygous108636525
1264699702264699703AG35GENIChomozygous108636526
1264699848264699849CT37GENIChomozygous108636527
1264699932264699933GA30GENIChomozygous108636528
1264700403264700404CA28GENIChomozygous108636529
1264702741264702742CT25GENIChomozygous108636532
1264702993264702994TC14GENIChomozygous108636533
1264708450264708451TA28GENIChomozygous108636541
1264708580264708581TA28GENIChomozygous108636542
1264708987264708988TC17GENIChomozygous108636543
1264710359264710360AG8GENIChomozygous108636544
1264710979264710980GC28GENIChomozygous108636545
1264711219264711220GC19GENIChomozygous108636546
1264711608264711609AG24GENIChomozygous108636547
1264712749264712750GA15GENIChomozygous108636548
1264712959264712960AG30GENIChomozygous108636549
1264718182264718183CT23GENIChomozygous108636550
1264720231264720232GA31GENIChomozygous108636553
1264721514264721515CT25GENIChomozygous108636554
1264723249264723250AG12GENIChomozygous108636556
1264725119264725120TA17GENIChomozygous108636557
1264725570264725571TC24GENIChomozygous108636558
1264727042264727043GT23GENIChomozygous108636559
1264728838264728839CT24GENIChomozygous108636560
1264729808264729809TA14GENIChomozygous108636561
1264731389264731390GA19GENIChomozygous108636562