chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160117220160117221GA12GENIChomozygous111791348
3160121364160121365TC22GENIChomozygous111791350
3160122035160122036AC10GENIChomozygous111791352
3160122802160122803TC19GENIChomozygous111791354
3160125087160125088TC19GENIChomozygous111791356
3160125187160125188CT12GENIChomozygous111791358
3160125819160125820GA20GENIChomozygous111791366
3160125987160125988AG12GENIChomozygous111791368
3160126282160126283GA4GENIChomozygous125840819
3160127632160127633TC9GENIChomozygous111791370
3160127970160127971AG12GENIChomozygous111791372
3160130184160130185AT19GENIChomozygous111791376
3160131879160131880TC21GENIChomozygous111791378
3160134869160134870CT14GENIChomozygous111791386
3160134924160134925GA21GENIChomozygous111791388
3160134959160134960GA22GENIChomozygous111791390
3160135993160135994CT4GENIChomozygous111791392
3160136512160136513AC5GENICheterozygous125840820
3160136723160136724CT24GENIChomozygous111791394
3160139923160139924TA5GENIChomozygous111791396