chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71861834418618345AAAG9GENIChomozygous53813816
71862306918623070CG17GENICpossibly homozygous53813819
71862407918624080TC9GENIChomozygous53813820
71863203918632040T-6GENIChomozygous53813826
71863227018632271GA7GENICpossibly homozygous53813827
71863370618633707TA24GENIChomozygous53813828
71863576318635764AG28GENIChomozygous53813829
71863749318637494AG27GENIChomozygous53813830
71863817818638179AAT2GENIChomozygous53813831
71863820818638210AC--2GENIChomozygous53813832
71863933918639341CA--6GENICheterozygous54636822
71864073518640736CT10GENIChomozygous53813834
71864476318644764AAACAC1GENIChomozygous53813838
71864581518645816GA4GENIChomozygous53813843
71864759218647593T-21GENIChomozygous53813846
71864998318649984AT14GENICpossibly homozygous53813847
71865103218651033GA21GENIChomozygous53813848
71865193218651933CT26GENIChomozygous53813852
71865227118652272TC14GENICpossibly homozygous53813853
71865977718659778CT17GENICpossibly homozygous53813861
71866045318660454GA26GENICpossibly homozygous53813862
71866530418665305TA15GENIChomozygous53813868
71866741418667415AG30GENICpossibly homozygous53813869
71863485518634856A-2GENIChomozygous54558633