chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160117220160117221GA40GENIChomozygous111791348
3160121364160121365TC42GENIChomozygous111791350
3160122035160122036AC38GENIChomozygous111791352
3160122802160122803TC70GENIChomozygous111791354
3160125087160125088TC48GENIChomozygous111791356
3160125187160125188CT45GENIChomozygous111791358
3160125308160125309TC35GENIChomozygous111791360
3160125558160125559CT22GENICheterozygous111791362
3160125600160125601CT29GENICheterozygous111791364
3160125819160125820GA40GENIChomozygous111791366
3160125987160125988AG61GENIChomozygous111791368
3160127632160127633TC42GENIChomozygous111791370
3160127970160127971AG52GENIChomozygous111791372
3160128055160128056GA54GENIChomozygous111791374
3160130184160130185AT54GENICpossibly homozygous111791376
3160131879160131880TC59GENIChomozygous111791378
3160133271160133272CT20GENICheterozygous111791380
3160133400160133401TA17GENIChomozygous111791382
3160133404160133405TA18GENIChomozygous111791384
3160134869160134870CT35GENIChomozygous111791386
3160134924160134925GA38GENIChomozygous111791388
3160134959160134960GA46GENIChomozygous111791390
3160135993160135994CT31GENIChomozygous111791392
3160136723160136724CT61GENIChomozygous111791394
3160139923160139924TA34GENICpossibly homozygous111791396