chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18543863485438635CT11GENICheterozygous402951571
18543863485438635C11GENICheterozygous402951572
18543863685438637CG11GENICheterozygous402951573
18543863685438637CT11GENICheterozygous402951574
18543863685438637C11GENICheterozygous402951575
18543863785438638CA11GENICheterozygous402951576
18543863785438638C11GENICheterozygous402951577
18543863885438639CG11GENICheterozygous140961890
18543864185438642CA12GENICheterozygous402951578
18543864185438642C12GENICheterozygous402951579
18543864385438644CT12GENICheterozygous402951580
18543864385438644C12GENICheterozygous402951581
18543864485438645CT12GENICheterozygous402951582
18543864485438645C12GENICheterozygous402951583
18544567285445673CT22GENICheterozygous140961891
18544567485445675GT21GENICheterozygous140961892
18544568185445682AC21GENICheterozygous147428096
18544569585445696AT22GENICheterozygous403969402
18544569585445696A22GENICheterozygous403969403
18544569585445696AG22GENICheterozygous403969404
18544567885445681AGA22GENICheterozygous147427306