chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5121763374121763375TC21GENIChomozygous122380401
5121763376121763376AG22GENIChomozygous128232407
5121763403121763404TG24GENIChomozygous114244562
5121763404121763405TC25GENIChomozygous114244563
5121824886121824887TA10GENICheterozygous130322619
5121846768121846768A18GENICheterozygous130552032
5121861343121861344CA4GENIChomozygous130322624
5121876576121876576G5GENIChomozygous128232482
5121876577121876577TTGCTA6GENIChomozygous128232483
5121876579121876580GC7GENIChomozygous128298482
5121876581121876581AGCG7GENIChomozygous128232484
5121876583121876584GC8GENIChomozygous128298483
5121876585121876585ACCAC8GENIChomozygous128232485
5121876588121876588GCTAAATCCCC7GENIChomozygous128232486
5121860083121860084AC4GENICheterozygous130555148
5121902640121902641TC9GENICheterozygous130555149
5121979868121979869C3GENIChomozygous130552033
5121989390121989391CG12GENIChomozygous113986053
5122005241122005242C6GENIChomozygous128232526
5122005760122005761AC37GENICheterozygous130555150
5122005784122005785TC37GENICheterozygous130555151
5122005807122005808GA29GENICheterozygous130555152
5122010470122010471GT17GENIChomozygous113986078
5122016682122016683AG27GENIChomozygous113986083
5122022019122022021AC7GENIChomozygous130552034
5122106471122106471GGGGGATGTTTGTCCGGAAACCG8GENIChomozygous128232549
5122106577122106578T24GENICheterozygous128232550
5122121273122121273A5GENICheterozygous130313747
5122121274122121275CA5GENICheterozygous113986235
5122121662122121666TAAA18GENIChomozygous128232551
5122121670122121672AG18GENIChomozygous128232552