chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105097862105097863CG67GENIChomozygous108905901
1105098036105098037CT54GENIChomozygous108905902
1105098212105098213CT63GENIChomozygous108905903
1105098340105098341GA64GENIChomozygous108905904
1105099604105099605CT42GENIChomozygous108905905
1105099710105099711AG53GENIChomozygous108905906
1105100184105100185CT52GENIChomozygous108905907
1105100832105100833AG54GENIChomozygous108905908
1105101832105101833TC48GENIChomozygous108905909
1105103632105103633TC31GENIChomozygous108905910
1105103652105103653TC37GENIChomozygous108905911
1105103919105103920GA39GENIChomozygous108905912
1105107551105107552AG64GENIChomozygous108905915
1105107638105107639AG55GENIChomozygous108905916
1105107943105107944TC43GENIChomozygous108905917
1105108957105108958TC54GENIChomozygous108905918
1105108293105108293T26GENIChomozygous130819268
1105105239105105241TG25GENICheterozygous127409935
1105105543105105543C52GENIChomozygous130819266
1105105929105105943GTGTGGTGTCACTT50GENIChomozygous130819267