chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1294472659447266AG37GENIChomozygous115251092
1294473069447307TG35GENIChomozygous115251094
1294473359447336GA33GENIChomozygous115251096
1294473599447360CT37GENIChomozygous115251098
1294477239447724GA79GENIChomozygous115251100
1294478079447808AC57GENIChomozygous115251102
1294492289449229GA27GENICpossibly homozygous115251104
1294512959451296CT60GENIChomozygous115464714
1294518939451894AG38GENIChomozygous115251106
1294519369451937GC48GENICheterozygous118243257
1294519799451980CT43GENIChomozygous115360311
1294522579452258GA43GENIChomozygous115251108
1294522959452296TA38GENIChomozygous115444964
1294525159452516GA21GENIChomozygous115251110
1294526199452620AG9GENIChomozygous115580079
1294526939452694GA35GENIChomozygous115251112
1294526999452700CT34GENIChomozygous115251114
1294529149452915AG42GENIChomozygous115444966
1294530209453021GA42GENIChomozygous115251116
1294530849453085GA48GENIChomozygous115251118
1294531499453150GT40GENIChomozygous115251120
1294537709453771TA53GENIChomozygous115251122
1294543849454385GA53GENIChomozygous115251124
1294544069454407AG57GENIChomozygous115251126
1294547089454709AG41GENIChomozygous115251128
1294547869454787GC31GENICheterozygous118243258
1294550129455013TA36GENIChomozygous115251130
1294551639455164AT51GENIChomozygous115251132
1294554699455470GA49GENIChomozygous115251134