chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224572733224572734CT21GENIChomozygous663284042
4224573209224573210TC22GENIChomozygous663284043
4224573259224573261TG--19GENIChomozygous765060118
4224573304224573305TG24GENIChomozygous663284044
4224573816224573817TTC22GENIChomozygous765060120
4224574455224574456TC36GENIChomozygous663284045
4224575209224575210TC21GENIChomozygous663284046
4224575442224575443T-15GENIChomozygous765060122
4224575513224575525TCTCTCTCTCTC------------4GENIChomozygous765060123
4224575578224575579AG7GENIChomozygous663284047
4224575699224575700GGA18GENIChomozygous765060125
4224575702224575703AT19GENIChomozygous663284048
4224575703224575704CCTTATGAGTGT19GENIChomozygous765060126
4224575704224575705CT19GENIChomozygous663284049
4224576326224576327AC27GENIChomozygous663284050
4224576402224576403GA37GENIChomozygous663284051
4224576561224576562TG20GENIChomozygous663284052
4224576594224576595AT16GENIChomozygous663284053
4224576851224576852AG17GENIChomozygous663284054
4224577057224577058CCA14GENIChomozygous765060127
4224577254224577255AG24GENIChomozygous663284055
4224577762224577766ACAG----23GENIChomozygous765060128
4224578284224578285A-14GENIChomozygous765060129
4224578306224578307AAAG18GENIChomozygous765060130
4224578387224578388AG21GENIChomozygous663284056
4224579990224579991TG10GENIChomozygous663284057
4224580805224580806GC25GENIChomozygous663284058