chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109106249991062500CG21GENIChomozygous553672368
109106390791063908GGGGTGGT14GENIChomozygous701612611
109106408491064100TGTGTGTGTGTGCGTG----------------3GENIChomozygous701612613
109106417391064174TC18GENIChomozygous555421329
109106430591064306CA27GENIChomozygous555421330
109106473491064735AG12GENIChomozygous553672369
109106510391065104CT19GENIChomozygous555421331
109106592991065930C-19GENIChomozygous701612614
109106671791066718GA32GENIChomozygous553672370
109106689591066896CT22GENIChomozygous555421332
109106722191067223TG--21GENIChomozygous701612615
109106778791067788TC24GENIChomozygous555421333
109106818591068186AAT14GENICpossibly homozygous701612616
109106864791068648CT23GENIChomozygous555421334
109106890491068905CT21GENIChomozygous553672371
109106950991069510GA20GENIChomozygous553672372
109106955291069553TC16GENIChomozygous553672373
109106973291069733AG18GENIChomozygous553672374
109106982491069825G-25GENIChomozygous701612617
109107004291070043GA27GENIChomozygous553672375
109107010691070107CCG5GENIChomozygous701612618
109107011291070116GAGA----8GENICheterozygous701612619
109107013391070135GA--7GENICpossibly homozygous701612623
109107033491070335CG21GENIChomozygous553672376
109107072991070731TG--24GENIChomozygous701612624
109107137491071375AG26GENIChomozygous553672377
109107167291071673TTA16GENIChomozygous701612625
109107210491072116TATTTATTTATT------------2GENIChomozygous701612626
109107222191072222AAT6GENIChomozygous701612630
109107268491072685A-2GENIChomozygous701612631
109107286591072866CA18GENIChomozygous553672378