chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X121580610121580611A-5INTERGENICheterozygous45329122
X121633150121633151CT20INTERGENICheterozygous45210799
X121655698121655699AG14INTERGENICheterozygous45210829
X121655881121655882AG19INTERGENICheterozygous45210830
X121656230121656231AG18INTERGENICheterozygous45210831
X121656461121656462CA36INTERGENICheterozygous45210832
X121656468121656469CA34INTERGENICheterozygous45210833
X121660203121660204GT11INTERGENICheterozygous45210846
X121661733121661734CT5INTERGENICheterozygous45329123
X121618599121618601TG--6INTERGENIChomozygous45314103
X121648378121648380TC--4INTERGENIChomozygous45314105
X121672234121672235GA7INTERGENICheterozygous45210870
X121674513121674514T-7INTERGENICheterozygous45329124
X121688399121688403TGTG----5INTERGENICheterozygous45210886
X121694366121694367TTCCACCTC5INTERGENIChomozygous45210894
X121702225121702226AC9INTERGENICpossibly homozygous45210907
X121703351121703352T-3INTERGENIChomozygous45314109
X121713824121713825AT5INTERGENIChomozygous45210921
X121714784121714785CCAA2INTERGENICheterozygous45210925
X121724708121724709CT10GENICheterozygous45314110
X121733357121733358AC5GENICheterozygous45210972
X121733362121733363AC5GENICheterozygous45210973
X121733363121733364AC5GENICheterozygous45210974