chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1189516499189516500TC40GENIChomozygous108976855
1189516624189516625GT43GENIChomozygous108976858
1189516995189516996CT44GENIChomozygous108976859
1189517051189517052TG43GENIChomozygous120488509
1189517214189517215AC41GENIChomozygous108976860
1189517519189517520GA38GENIChomozygous108976861
1189517530189517531AT40GENIChomozygous108976862
1189517817189517818TC38GENIChomozygous108976864
1189518032189518033AC48GENIChomozygous108976865
1189518336189518337CG41GENIChomozygous108976867
1189518349189518350TC41GENIChomozygous108976868
1189518385189518386GT33GENIChomozygous108976869
1189520693189520694AG39GENIChomozygous108976871
1189520740189520741CG41GENIChomozygous108976872
1189520960189520961TA48GENIChomozygous108976873
1189522134189522135GA52GENIChomozygous108976875
1189524774189524775TC43GENIChomozygous108976876
1189524911189524912CT42GENIChomozygous108976877
1189525550189525551GA37GENIChomozygous108976879
1189527492189527493GC29GENIChomozygous108976880
1189527712189527713CG19GENIChomozygous108976881
1189528331189528332GC18GENIChomozygous120488510
1189529457189529458TC25GENIChomozygous108976882
1189531325189531326CT17GENIChomozygous108976883
1189531495189531496AC19GENIChomozygous120475139
1189530101189530102CT20GENIChomozygous108463974
1189531734189531735TG15GENIChomozygous108463977
1189532485189532486GA25GENIChomozygous108976884
1189533753189533754CT23GENIChomozygous108463982
1189534247189534248CT22GENIChomozygous108976885
1189534579189534580TC27GENIChomozygous108463983
1189534703189534704AG38GENIChomozygous108463984
1189537604189537605CT25GENIChomozygous108763487
1189537605189537606TC25GENIChomozygous120475141
1189538220189538221CT16GENIChomozygous108976887
1189538267189538268CT19GENIChomozygous108463992
1189540173189540174AG24GENIChomozygous108463994
1189540372189540373AG15GENIChomozygous108463995
1189541084189541085AG9GENIChomozygous108976888