chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139291650692916507G10GENICheterozygous66920966
139291652792916528AG7GENIChomozygous67371815
139291656592916566GC6GENIChomozygous66641600
139291656692916567CA6GENIChomozygous66641603
139292033392920334AT6GENIChomozygous67371816
139292128492921285CT19GENIChomozygous67331177
139292179192921792CG7GENIChomozygous67371817
139292234292922343AG13GENIChomozygous67331181
139292240592922406CT12GENIChomozygous67331183
139292290292922903T9GENICheterozygous67331185
139292449292924493AT27GENIChomozygous67371818
139292531092925311AG19GENIChomozygous67331189
139292891192928912AG7GENIChomozygous67371820
139292986692929867GA14GENIChomozygous67371822
139293087992930880GA12GENIChomozygous67371823
139293180992931810CT4GENIChomozygous67371824
139293313692933137GT9GENIChomozygous67371825
139293408692934087C15GENICheterozygous67371827
139291661892916619T18GENICheterozygous66880187
139292362592923626AG6GENIChomozygous66880190
139291764292917642A8GENICheterozygous67538526
139293351292933513CG4GENIChomozygous67538527
139293178392931784AG6GENIChomozygous67122443