chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116928822116928823AC40GENIChomozygous115845859
7116930571116930572TC38GENIChomozygous115845861
7116930772116930773T30GENIChomozygous128510394
7116930950116930951TC40GENIChomozygous115845863
7116931640116931641TC30GENIChomozygous115845865
7116932522116932523GA46GENIChomozygous115845867
7116932532116932533GA46GENIChomozygous115845869
7116933057116933058AT47GENIChomozygous115845871
7116933972116933973AG43GENIChomozygous115845873
7116934411116934412GA45GENIChomozygous115845875
7116935780116935781GT55GENIChomozygous115845877
7116937285116937286GT49GENIChomozygous115845879
7116939505116939505CTG48GENIChomozygous128510395
7116939739116939740TG48GENIChomozygous115845881
7116941317116941318TC48GENIChomozygous115845883
7116941522116941523AG37GENIChomozygous115845885
7116941528116941529TA35GENIChomozygous115845887
7116941529116941530CA35GENIChomozygous115845889
7116941685116941686A43GENIChomozygous128510396
7116941720116941721CA39GENIChomozygous115845891
7116941721116941722TG39GENIChomozygous115845893