chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155400557054005571TA45GENIChomozygous65114235
155400630154006302GC40GENIChomozygous65114236
155400638454006385TG43GENIChomozygous65114237
155400794454007945AG77GENICpossibly homozygous65114238
155400810054008101TG18GENICheterozygous65114239
155400819254008193GA80GENICheterozygous65114240
155400821554008216TG90GENICheterozygous65114241
155400931754009318GC43GENIChomozygous65114242
155401025754010258AG30GENIChomozygous65114243
155401030654010307GA36GENIChomozygous65114244
155401248554012486CT38GENIChomozygous65114245
155401358054013581CT45GENIChomozygous65114246
155401436154014362GA47GENIChomozygous65114247
155401462854014629TC19GENICpossibly homozygous65114248
155401481854014819CT37GENIChomozygous65114249
155401522454015225TC48GENIChomozygous65114250
155401539554015396CT33GENIChomozygous65114251
155401541254015413TA31GENIChomozygous65114252
155401580354015804TC40GENIChomozygous65114253
155401609154016092AT31GENIChomozygous65114254
155401617854016179GA24GENIChomozygous65114255
155401643654016437TC50GENIChomozygous65114256
155401666554016666AT27GENIChomozygous65114257
155401686454016865CA37GENIChomozygous65114258
155401800854018009AT42GENIChomozygous65114259
155401830254018303AG49GENIChomozygous65114260
155401839454018395AT67GENICpossibly homozygous65114261
155402063554020636AT53GENIChomozygous65114262
155402070254020703CT48GENIChomozygous65114263
155402107154021072CT38GENIChomozygous65114264
155402157554021576AT49GENIChomozygous65114265
155402192554021926GA31GENIChomozygous65114266
155402279554022796CT22GENIChomozygous65114267
155402339754023398GT49GENIChomozygous65114268
155402409554024096AG45GENIChomozygous65114269
155402441154024412CA53GENIChomozygous65114270
155402451354024514CT44GENICpossibly homozygous65114271
155402590754025908CT25GENIChomozygous65114272
155402680354026804AT16GENIChomozygous65114273