chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1189350772189350773AG101GENICheterozygous108463886
1189350802189350803GA102GENICheterozygous108463887
1189350824189350825AG106GENICheterozygous108463888
1189350940189350941CT119GENICheterozygous108463889
1189351483189351484AG99GENICheterozygous109176127
1189351914189351915CG73GENICheterozygous108463890
1189351918189351919CG74GENICheterozygous108463891
1189351922189351923CG79GENICheterozygous108463892
1189352071189352072GA87GENICheterozygous108463893
1189352178189352179AC84GENICheterozygous108463894
1189352194189352195AG89GENICheterozygous108463895
1189352368189352369CT83GENICheterozygous108463896
1189352621189352622TC86GENICheterozygous108463897
1189352638189352639CT78GENICheterozygous108463898
1189352674189352675AC63GENICheterozygous108763456
1189353704189353705TG32GENIChomozygous108463899
1189356401189356402TC2GENIChomozygous109176129
1189356626189356627GT10GENIChomozygous108463901
1189357295189357296CT24GENIChomozygous108463902
1189364118189364119CG29GENIChomozygous108976496