chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76071911460719115CA15GENIChomozygous116177738
76071922960719230GA16GENIChomozygous116332186
76071947860719479GA12GENIChomozygous116332187
76071970560719706TA19GENIChomozygous116177740
76071975660719757TA20GENIChomozygous116177742
76071976760719768AG16GENIChomozygous116177744
76071978960719790GA10GENIChomozygous116177746
76072076860720769CT19GENIChomozygous116177748
76072137860721379GT4GENIChomozygous116177750
76072168460721685CT10GENIChomozygous116177752
76072188160721882CT23GENIChomozygous116177756
76072281560722816GA21GENIChomozygous116332188
76072351460723515AG19GENIChomozygous116177767
76072477860724779AC20GENIChomozygous116177771
76072487260724873GA14GENIChomozygous116177773
76072583360725834TC21GENIChomozygous116177777
76072593660725937CA27GENIChomozygous116332190
76072649160726492AT19GENIChomozygous116177781
76072687960726880AG15GENIChomozygous116177783
76072733560727336CT18GENIChomozygous116332191
76072768060727681CG18GENIChomozygous116177793
76072770760727708CT20GENIChomozygous116177795
76072818160728182GC14GENIChomozygous116177797
76073032760730328TG25GENIChomozygous116332195
76073064260730643TC21GENIChomozygous116332196
76073109360731094GA26GENIChomozygous116332197
76073226160732262TC17GENIChomozygous116177799
76073247960732480GA20GENIChomozygous116177801
76073469960734700CT23GENIChomozygous118338771
76073589760735898CA23GENIChomozygous116177807
76073644160736442GT28GENIChomozygous116177809
76073776360737764CT13GENIChomozygous116177813
76073959060739591CT10GENIChomozygous116332203
76074029560740296AG26GENIChomozygous116177817
76074239260742393CT16GENIChomozygous116177827
76074337060743371AG4GENIChomozygous116177833