chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2116107054116107055TG10GENICheterozygous125580501
2116107547116107548AG23GENIChomozygous109989126
2116135600116135601AT8GENIChomozygous125722061
2116143814116143815TC9GENIChomozygous109989166
2116146442116146443CG9GENIChomozygous125628679
2116146646116146647GA17GENIChomozygous125580505
2116148192116148193TC12GENIChomozygous109989168
2116150945116150946AG13GENIChomozygous109989172
2116148486116148487TC12GENIChomozygous109989169
2116150802116150803CG15GENIChomozygous109989171
2116152357116152358GC13GENIChomozygous120442846
2116152524116152525CT20GENIChomozygous120442847
2116154649116154650GC16GENIChomozygous120442850
2116154864116154865CT10GENIChomozygous120442851
2116155570116155571TC13GENIChomozygous109989174
2116155595116155596AG8GENIChomozygous109989175
2116155998116155999AT16GENIChomozygous109989176
2116156203116156204AG14GENIChomozygous109989177
2116156267116156268GA8GENIChomozygous109989178
2116156281116156282TC10GENIChomozygous120442852
2116157202116157203TC21GENIChomozygous109989179
2116157258116157259CG11GENIChomozygous120442853
2116158084116158085CT28GENIChomozygous120442854
2116158819116158820TA6GENIChomozygous109989180
2116160646116160647AT7GENICheterozygous125580507