chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1189516624189516625GT10GENIChomozygous108976858
1189517630189517631TC14GENIChomozygous108976863
1189522555189522556GA22GENIChomozygous109176247
1189525170189525171CT23GENIChomozygous109176249
1189526125189526126AG9GENIChomozygous109176253
1189527492189527493GC18GENIChomozygous108976880
1189528331189528332GC18GENIChomozygous120488510
1189529457189529458TC13GENIChomozygous108976882
1189529825189529826GA6GENIChomozygous109176255
1189530224189530225CT9GENIChomozygous109176257
1189530656189530657GA7GENIChomozygous109176259
1189531495189531496AC8GENIChomozygous120475139
1189531734189531735TG9GENIChomozygous108463977
1189530101189530102CT6GENIChomozygous108463974
1189533753189533754CT10GENIChomozygous108463982
1189534579189534580TC10GENIChomozygous108463983
1189534703189534704AG15GENIChomozygous108463984
1189535136189535137CT35GENIChomozygous108463985
1189537092189537093AT26GENIChomozygous120475140
1189537126189537127TC28GENIChomozygous108463990
1189537316189537317GA14GENIChomozygous108463991
1189537604189537605CT14GENIChomozygous108763487
1189537605189537606TC14GENIChomozygous120475141
1189540173189540174AG18GENIChomozygous108463994
1189538267189538268CT11GENIChomozygous108463992
1189538517189538518GA6GENIChomozygous108463993
1189540372189540373AG18GENIChomozygous108463995
1189540795189540796TC16GENIChomozygous108463996
1189541104189541105TC20GENIChomozygous108463997