chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137392976273929763AT28GENIChomozygous50258939
137392979673929797AC25GENICpossibly homozygous49814534
137393035073930351GA12GENIChomozygous49814537
137393143173931432GA1GENIChomozygous49814540
137393172073931721T-1GENIChomozygous49814544
137393236073932361GGGTTTTTTTTTTTTTTTTTTTTTTTTT3GENIChomozygous50522933
137393294373932944GA19GENICpossibly homozygous50092545
137393364073933641GA22GENICpossibly homozygous50258943
137393493673934937AG7GENIChomozygous50258945
137393518673935187TA3GENICheterozygous50258949
137393528673935287TC3GENIChomozygous50258953
137393569573935696TC12GENIChomozygous49814565
137393817473938175TTAC3GENICheterozygous49814569
137393823773938238TC12GENIChomozygous49814570
137393836173938362AG17GENIChomozygous50258955
137393904573939046CT16GENIChomozygous50258957
137394023873940239AC16GENIChomozygous50258961
137394037573940378CTT---12GENICheterozygous50258963
137394043473940435AC30GENIChomozygous49814576
137394081973940820TC6GENIChomozygous50258965
137394083173940832AATTCAGAG4GENIChomozygous50258967
137394116473941165GA18GENIChomozygous50258969
137394142573941426AG21GENIChomozygous49814578
137394143473941435AG16GENIChomozygous50258971
137394147873941479AG16GENIChomozygous49814580
137394148073941481AG15GENIChomozygous50258973