chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125184616951846173ATGG----20INTERGENIChomozygous50247945
125184793851847939C-21INTERGENIChomozygous50514145
125184794851847949CA25INTERGENIChomozygous50514147
125185008651850087GC22GENIChomozygous50247949
125185040851850409CA16GENIChomozygous50247951
125185056351850564AG18GENIChomozygous50247953
125185063251850633CT11GENIChomozygous50247955
125185064551850646AG8GENIChomozygous50247957
125185099651850997TC14GENIChomozygous50247959
125185238651852387GT13GENIChomozygous50247961
125185238751852388GT14GENIChomozygous50247963
125185298551852989CCCT----12GENIChomozygous50247965
125185395351853954AG28GENIChomozygous50247967
125187046051870468CTAGGTTA--------18GENIChomozygous50247969
125187085451870855AG23GENIChomozygous50247971
125187138951871390CT11GENIChomozygous50247973
125187159951871600TC23GENIChomozygous50247975
125187170251871703TC20GENIChomozygous50247977
125187172851871729GA21GENIChomozygous50247979
125187230651872307T-18GENIChomozygous50247983
125187249251872493GT19GENIChomozygous50247985
125187283651872837AG23GENIChomozygous50247987
125187308551873089TCGA----29GENICpossibly homozygous50247989
125187324951873250AG39GENIChomozygous50247991
125187358651873587TC21GENIChomozygous50247993
125187398551873986CCAG9GENIChomozygous50248004
125187409951874100TC11GENIChomozygous50248006
125187415851874159GA16GENIChomozygous50248008
125187510551875106TC3GENIChomozygous50248010
125187519551875196GA9GENIChomozygous50248012
125187520151875202GA10GENIChomozygous50248014
125187531551875316GGAGAGAGAGAGAGAT10GENICpossibly homozygous50514149
125187571451875715GA26GENIChomozygous50248018
125187599451875995AG10GENIChomozygous50248020
125187700551877006TTC20GENIChomozygous50248045
125187794851877949TC26GENIChomozygous50248047
125187628451876288TTAT----3GENIChomozygous50547389
125187388751873888GGAGAGAGAGAGAGAGAGAGAGAGAGACAGAGACAGAGAC9GENIChomozygous50547387
125187627551876277TT--2GENIChomozygous50547388