chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105097046105097047CT3GENIChomozygous108905899
1105097056105097057AG1GENIChomozygous108905900
1105097862105097863CG18GENIChomozygous108905901
1105098036105098037CT16GENIChomozygous108905902
1105098212105098213CT12GENIChomozygous108905903
1105098340105098341GA15GENIChomozygous108905904
1105099604105099605CT17GENIChomozygous108905905
1105099710105099711AG17GENIChomozygous108905906
1105100184105100185CT15GENIChomozygous108905907
1105100832105100833AG12GENIChomozygous108905908
1105101832105101833TC20GENIChomozygous108905909
1105103632105103633TC8GENIChomozygous108905910
1105103652105103653TC9GENIChomozygous108905911
1105103919105103920GA11GENIChomozygous108905912
1105107551105107552AG18GENIChomozygous108905915
1105107638105107639AG23GENIChomozygous108905916
1105107943105107944TC11GENIChomozygous108905917
1105108957105108958TC11GENIChomozygous108905918
1105108293105108293T5GENIChomozygous130819268
1105105239105105241TG17GENICheterozygous127409935
1105105543105105543C19GENIChomozygous130819266
1105105929105105943GTGTGGTGTCACTT16GENIChomozygous130819267