chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
165400091554000916GA13GENIChomozygous777554402
165400258154002582AG28GENIChomozygous777554403
165400352154003522AC31GENIChomozygous777554404
165400380954003810CT34GENIChomozygous777554405
165400726754007268TC47GENICpossibly homozygous777554406
165400826354008264GA89GENICheterozygous777554407
165400826954008270AG85GENICheterozygous777554408
165400917354009174CA27GENIChomozygous777554409
165401112554011126AG59GENICpossibly homozygous777554410
165401315054013151AG34GENICpossibly homozygous777554411
165401370254013703TA65GENIChomozygous777554412
165401524754015248TC53GENIChomozygous777554413
165401555654015557AG33GENIChomozygous777554414
165401822654018227AG35GENICpossibly homozygous777554415
165402366154023662TC56GENIChomozygous777554416
165402504854025049AC17GENIChomozygous777554417
165402639454026395TG24GENIChomozygous777554418
165402646454026465CT35GENICpossibly homozygous777554419
165402646854026469AG33GENIChomozygous777554420
165402800154028002GA46GENIChomozygous777554421
165402841554028416TC48GENIChomozygous777554422
165402851754028518CT61GENICpossibly homozygous777554423
165402966954029670CT36GENIChomozygous777554424
165402970554029706CT35GENIChomozygous777554425