chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
389829848982985GA16GENIChomozygous111442594
389835598983560CT22GENIChomozygous111442595
389836258983626CG15GENIChomozygous111442596
389842678984268TA20GENIChomozygous111442597
389843058984306TA28GENIChomozygous111442598
389850278985028AG15GENIChomozygous111442599
389855698985570A13GENIChomozygous127848099
389869088986909GA21GENICpossibly homozygous111442601
389870278987028GC23GENIChomozygous112405609
389870298987029G23GENIChomozygous127848100
389876288987629CA18GENICpossibly homozygous111442606
389883348988335CG30GENICpossibly homozygous111442610
389893458989346TC17GENIChomozygous111442611
389906338990634TC22GENIChomozygous111442612
389923788992379AG22GENIChomozygous111442613
389926378992638AG31GENIChomozygous111442614
389948468994847GA25GENIChomozygous111442615
389973408997341AG20GENIChomozygous111442616
389982298998230GA21GENIChomozygous111442617
390029759002976CT23GENIChomozygous111442619
390034199003420GA28GENIChomozygous111442620
390049659004966TG12GENIChomozygous111442621
390056459005646A19GENIChomozygous127848107
389955918995591AAGG18GENIChomozygous127848102
389979498997950A24GENIChomozygous127848103
389984498998449G23GENIChomozygous127848104
389987568998757T21GENIChomozygous127848105
389990558999055TG18GENIChomozygous127848106
389988578998858GA33GENIChomozygous120076870
390056899005690GA22GENIChomozygous111442622
390065329006533TC14GENIChomozygous111442623
390065749006590AGGCTGGTCCCCAGGC12GENIChomozygous127848108
390094699009470AG28GENIChomozygous111442627
390068469006847TC16GENIChomozygous111442624
390078889007889CT11GENIChomozygous111442625
390087439008744CT20GENIChomozygous111442626
390096289009629TC14GENIChomozygous111442628
390107119010712CT18GENIChomozygous111442629
390111229011123GA19GENIChomozygous111442630