chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2050631635063164AG34GENIChomozygous109076322
2050633745063375AG31GENIChomozygous109076324
2050635105063511AT45GENICpossibly homozygous109455454
2050635225063523AT50GENICpossibly homozygous109390161
2050635865063587CA58GENIChomozygous109076330
2050636935063694CT44GENIChomozygous109461579
2050637445063745CT31GENIChomozygous109461580
2050638955063896TC25GENIChomozygous109076332
2050640345064035TA19GENIChomozygous109076334
2050645155064516GA22GENICpossibly homozygous109455456
2050653465065347CT28GENIChomozygous109076340
2050657055065706GA30GENIChomozygous109076344
2050659105065911GA27GENICheterozygous119858444
2050659625065963GA28GENIChomozygous109076346
2050659995066000GT38GENIChomozygous109076348
2050660325066033GA38GENIChomozygous109076350
2050662605066261AG21GENIChomozygous109076352
2050662715066272TC18GENIChomozygous109076354
2050662825066283GC20GENIChomozygous109076356
2050666555066656AG34GENIChomozygous109076358
2050669235066924AC15GENIChomozygous109076360
2050670525067053CT34GENIChomozygous109076364
2050670955067096GA35GENIChomozygous109076366
2050671325067133GA36GENIChomozygous109076368
2050671935067194CT40GENIChomozygous109076373
2050673635067364GC34GENIChomozygous109076375
2050675825067583GA34GENIChomozygous109076377
2050676365067637CT32GENIChomozygous109076379
2050677535067754AG16GENIChomozygous109076381
2050680245068025GA48GENIChomozygous109076385
2050684175068418TC25GENIChomozygous109076387
2050684595068460GA25GENIChomozygous109076389
2050685175068518AG30GENIChomozygous109076391
2050685445068545CG34GENIChomozygous109076393
2050686085068609CT35GENIChomozygous109076395
2050686745068675GC28GENIChomozygous109076397
2050687195068720AC19GENIChomozygous109076402
2050687465068747CT13GENIChomozygous109076405
2050688555068856AC36GENICpossibly homozygous109076409