chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160117220160117221GA55GENIChomozygous111791348
3160121364160121365TC61GENIChomozygous111791350
3160122035160122036AC48GENIChomozygous111791352
3160122802160122803TC66GENIChomozygous111791354
3160125087160125088TC71GENIChomozygous111791356
3160125187160125188CT46GENIChomozygous111791358
3160125308160125309TC49GENIChomozygous111791360
3160125558160125559CT42GENICheterozygous111791362
3160125819160125820GA51GENIChomozygous111791366
3160125987160125988AG47GENIChomozygous111791368
3160127632160127633TC48GENICpossibly homozygous111791370
3160127970160127971AG64GENIChomozygous111791372
3160128055160128056GA60GENIChomozygous111791374
3160130184160130185AT61GENIChomozygous111791376
3160131879160131880TC61GENIChomozygous111791378
3160133271160133272CT34GENICpossibly homozygous111791380
3160133400160133401TA42GENIChomozygous111791382
3160133404160133405TA46GENIChomozygous111791384
3160134869160134870CT48GENIChomozygous111791386
3160134924160134925GA49GENIChomozygous111791388
3160134959160134960GA40GENICpossibly homozygous111791390
3160135993160135994CT62GENICpossibly homozygous111791392
3160136723160136724CT49GENIChomozygous111791394
3160139923160139924TA43GENIChomozygous111791396