chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2199834380199834381GT30GENICpossibly homozygous111155683
2199835419199835420AG34GENIChomozygous110203391
2199835457199835458TG30GENIChomozygous110203392
2199835546199835547AG20GENIChomozygous110203393
2199836451199836452TC18GENICpossibly homozygous110203394
2199836479199836480AG28GENICpossibly homozygous110203395
2199836586199836587CT18GENICpossibly homozygous111155685
2199836927199836928CT24GENIChomozygous110203398
2199836990199836991AG23GENIChomozygous110203399
2199837583199837584GT23GENIChomozygous110203401
2199837596199837597CT24GENIChomozygous110203402
2199837639199837640TC25GENIChomozygous110203403
2199837797199837798TC26GENIChomozygous110203404
2199838363199838364AC38GENICpossibly homozygous110203405
2199838471199838472GA22GENIChomozygous110203406
2199838573199838574GA21GENICheterozygous110203407
2199838975199838976AG36GENICpossibly homozygous110203408
2199839475199839476CT30GENICpossibly homozygous111155687
2199840484199840485CT39GENICpossibly homozygous110203410
2199840655199840656GA25GENICpossibly homozygous110203411
2199841758199841759CT19GENIChomozygous111155689
2199841948199841949AG30GENICpossibly homozygous110203412
2199842101199842102TC32GENICpossibly homozygous110203413
2199842120199842121GA33GENICpossibly homozygous110203414
2199842747199842748AG17GENIChomozygous110203415
2199844392199844393TA15GENICpossibly homozygous110203419
2199844398199844399TC15GENICpossibly homozygous110203420
2199844597199844598AG23GENICpossibly homozygous110203422
2199844955199844956AG17GENIChomozygous111155691
2199845026199845027CG22GENICpossibly homozygous110203423
2199845162199845163CG32GENIChomozygous110203425
2199845668199845669GA23GENICpossibly homozygous110203426
2199845702199845703CG29GENIChomozygous110203427
2199845794199845795TA23GENICpossibly homozygous110203428
2199846135199846136AC21GENIChomozygous111155693