chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126896500126896501TC38GENIChomozygous113999404
5126896521126896522TC37GENIChomozygous113999406
5126896855126896856TG51GENIChomozygous113999408
5126897157126897158CA45GENICpossibly homozygous113999410
5126897943126897944TC29GENIChomozygous113999420
5126898814126898815GA45GENIChomozygous113999422
5126898853126898854TC54GENIChomozygous113999424
5126899746126899747TC56GENIChomozygous113999426
5126899951126899952CG50GENIChomozygous113999428
5126900060126900061GA49GENIChomozygous113999430
5126900946126900947GC45GENIChomozygous113999436
5126902001126902002AG31GENIChomozygous113999438
5126903167126903168GA53GENIChomozygous113999440
5126903399126903400CT32GENIChomozygous113999442
5126903813126903814TC46GENIChomozygous113999444
5126904348126904349AG52GENIChomozygous113999446
5126904442126904443AG44GENIChomozygous113999448
5126904842126904843AG24GENIChomozygous113999450
5126904848126904849CT24GENIChomozygous113999452
5126905073126905074CT36GENIChomozygous113999454
5126905107126905108GA37GENIChomozygous113999456
5126905988126905989CT22GENIChomozygous113999472
5126906071126906072AG37GENIChomozygous113999474
5126906755126906756GA38GENIChomozygous113999476
5126907612126907613TC40GENIChomozygous113999492
5126907977126907978CT25GENIChomozygous113999494
5126908245126908246GA46GENIChomozygous113999496
5126908315126908316CT38GENIChomozygous113999498
5126908712126908713AG44GENIChomozygous113999502
5126909612126909613TC48GENICpossibly homozygous113999504
5126909690126909691CT45GENIChomozygous113999506
5126910279126910280CT38GENIChomozygous113999508
5126910514126910515GA38GENIChomozygous113999510
5126910859126910860AG41GENIChomozygous113999512