chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227404236227404237AG13GENIChomozygous108999124
1227404464227404465AG23GENIChomozygous108999126
1227404511227404512CA19GENIChomozygous108999127
1227404565227404566AT15GENIChomozygous108999128
1227404931227404932AG10GENIChomozygous108999129
1227405046227405047GC15GENIChomozygous108999130
1227405143227405144TG14GENIChomozygous108999131
1227405402227405403TA17GENIChomozygous108999132
1227405827227405828CT21GENIChomozygous108999133
1227406133227406134CG22GENIChomozygous108999134
1227406383227406384TG17GENIChomozygous108999135
1227407118227407119TC20GENIChomozygous108999137
1227407406227407407AT13GENIChomozygous109199058
1227407407227407408AT13GENIChomozygous109199060
1227407520227407521TC16GENIChomozygous108999138
1227408030227408031CT28GENIChomozygous108999140
1227408084227408085TC23GENIChomozygous108999141
1227408316227408317CT19GENIChomozygous108999142
1227408424227408425GT21GENIChomozygous108999143
1227408563227408564AC22GENIChomozygous108999144
1227408845227408846CT29GENIChomozygous108999145
1227408860227408861AG29GENIChomozygous108999146
1227409038227409039AG18GENIChomozygous108999147
1227409520227409521AC29GENIChomozygous120512364
1227409521227409522GA28GENIChomozygous120512365
1227409551227409552CA26GENIChomozygous108999148
1227410130227410131TC26GENIChomozygous108999149
1227410145227410146TC30GENIChomozygous108999150
1227410406227410407AC28GENIChomozygous108999151
1227411765227411766AG22GENIChomozygous108999152
1227411975227411976AC16GENIChomozygous108999153
1227412211227412212TC22GENIChomozygous108999154
1227412235227412236AG18GENIChomozygous108999155
1227413022227413023CT24GENIChomozygous109199062
1227413211227413212GC16GENIChomozygous108999156
1227414517227414518GA9GENIChomozygous108999166
1227414676227414677CA5GENIChomozygous108999167