chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125184616951846173ATGG----11INTERGENICpossibly homozygous50247945
125184782751847828GT11INTERGENICheterozygous50473145
125184793851847939C-4INTERGENIChomozygous50514145
125184794851847949CA5INTERGENIChomozygous50514147
125185008651850087GC12GENICpossibly homozygous50247949
125185040851850409CA12GENIChomozygous50247951
125185056351850564AG11GENICpossibly homozygous50247953
125185063251850633CT9GENIChomozygous50247955
125185064551850646AG9GENICpossibly homozygous50247957
125185099651850997TC13GENIChomozygous50247959
125185238651852387GT25GENICheterozygous50247961
125185238751852388GT25GENICheterozygous50247963
125185298551852989CCCT----2GENICheterozygous50247965
125185395351853954AG17GENIChomozygous50247967
125187046051870468CTAGGTTA--------2GENICheterozygous50247969
125187085451870855AG19GENIChomozygous50247971
125187138951871390CT16GENICpossibly homozygous50247973
125187159951871600TC17GENIChomozygous50247975
125187170251871703TC22GENICpossibly homozygous50247977
125187172851871729GA17GENICpossibly homozygous50247979
125187230651872307T-10GENICheterozygous50247983
125187249251872493GT20GENICpossibly homozygous50247985
125187283651872837AG19GENICpossibly homozygous50247987
125187308551873089TCGA----8GENIChomozygous50247989
125187324951873250AG24GENIChomozygous50247991
125187358651873587TC12GENICheterozygous50247993
125187409951874100TC21GENIChomozygous50248006
125187415851874159GA15GENICpossibly homozygous50248008
125187510551875106TC3GENICheterozygous50248010
125187519551875196GA12GENIChomozygous50248012
125187520151875202GA12GENICpossibly homozygous50248014
125187531551875316GGAGAGAGAGAGAGAT2GENIChomozygous50514149
125187571451875715GA7GENIChomozygous50248018
125187599451875995AG10GENICheterozygous50248020
125187700551877006TTC10GENIChomozygous50248045
125187794851877949TC33GENIChomozygous50248047