chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137392976273929763AT17GENIChomozygous50258939
137392979673929797AC13GENIChomozygous49814534
137393035073930351GA11GENIChomozygous49814537
137393143173931432GA4GENICheterozygous49814540
137393294373932944GA11GENIChomozygous50092545
137393364073933641GA18GENIChomozygous50258943
137393493673934937AG8GENIChomozygous50258945
137393518673935187TA5GENICheterozygous50258949
137393520973935210TC2GENIChomozygous49814561
137393521473935215TC1GENIChomozygous50258951
137393528673935287TC3GENIChomozygous50258953
137393569573935696TC4GENIChomozygous49814565
137393817473938175TTAC1GENIChomozygous49814569
137393823773938238TC5GENIChomozygous49814570
137393836173938362AG6GENIChomozygous50258955
137393904573939046CT15GENIChomozygous50258957
137393236073932361GGGTTTTTTTTTTTTTTTTTTTTTTTTT2GENIChomozygous50522933
137394023873940239AC18GENIChomozygous50258961
137394037573940378CTT---10GENICheterozygous50258963
137394043473940435AC10GENIChomozygous49814576
137394081973940820TC4GENIChomozygous50258965
137394083173940832AATTCAGAG1GENIChomozygous50258967
137394116473941165GA14GENIChomozygous50258969
137394142573941426AG7GENIChomozygous49814578
137394143473941435AG7GENICpossibly homozygous50258971
137394147873941479AG2GENIChomozygous49814580
137394148073941481AG1GENIChomozygous50258973
137394058573940586GA13GENICheterozygous50781975