chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155400557054005571TA19GENIChomozygous65114235
155400638454006385TG12GENIChomozygous65114237
155400794454007945AG8GENIChomozygous65114238
155400931754009318GC25GENIChomozygous65114242
155401025754010258AG18GENIChomozygous65114243
155401030654010307GA24GENIChomozygous65114244
155401248554012486CT9GENIChomozygous65114245
155401358054013581CT22GENIChomozygous65114246
155401436154014362GA11GENIChomozygous65114247
155401462854014629TC8GENIChomozygous65114248
155401481854014819CT15GENIChomozygous65114249
155401522454015225TC20GENIChomozygous65114250
155401539554015396CT12GENIChomozygous65114251
155401541254015413TA8GENIChomozygous65114252
155401580354015804TC9GENIChomozygous65114253
155401609154016092AT6GENIChomozygous65114254
155401617854016179GA8GENIChomozygous65114255
155401643654016437TC16GENIChomozygous65114256
155401686454016865CA13GENIChomozygous65114258
155401800854018009AT17GENIChomozygous65114259
155401830254018303AG20GENIChomozygous65114260
155401839454018395AT18GENIChomozygous65114261
155401927554019275A16GENICheterozygous65715133
155400896754008974TCTCATT12GENICheterozygous65715125
155401015554010157GG13GENICheterozygous65715127
155401582854015829GA10GENIChomozygous65715129
155401583254015833AG9GENIChomozygous65715131
155402063554020636AT23GENIChomozygous65114262
155402070254020703CT26GENIChomozygous65114263
155402107154021072CT11GENIChomozygous65114264
155402339754023398GT12GENIChomozygous65114268
155402157554021576AT23GENIChomozygous65114265
155402409554024096AG18GENIChomozygous65114269
155402441154024412CA22GENIChomozygous65114270
155402451354024514CT10GENIChomozygous65114271
155402590754025908CT6GENIChomozygous65114272
155402732854027330GG8GENICheterozygous65715135