chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203543104203543105TC53GENIChomozygous135791215
1203543984203543985G25GENIChomozygous402979263
1203543984203543985GT25GENICheterozygous402979264
1203544403203544404GA64GENIChomozygous148214263
1203544727203544728CT64GENIChomozygous148214264
1203546977203546978CT69GENIChomozygous148214265
1203548131203548132TC70GENIChomozygous148214266
1203548827203548828GA96GENIChomozygous148214267
1203549526203549527CT82GENICpossibly homozygous148214268
1203551963203551964AG84GENIChomozygous148214269
1203552161203552162AG65GENIChomozygous135791225
1203553446203553447GT69GENIChomozygous148214270
1203555649203555650GC63GENIChomozygous135791230
1203556184203556185GT71GENICpossibly homozygous148214271
1203558385203558386CT73GENIChomozygous148214272
1203559263203559264TG34GENICpossibly homozygous153906426
1203559263203559264T34GENICheterozygous402979265
1203559368203559369CT46GENIChomozygous144260815
1203559078203559079GA17GENIChomozygous403702632
1203560856203560857GA49GENIChomozygous144260817
1203546046203546046A65GENIChomozygous135455535
1203546923203546927AAGA55GENIChomozygous148211073
1203561064203561068ATCC57GENIChomozygous135455538
1203561202203561203CA72GENIChomozygous144260818
1203561211203561212TC75GENIChomozygous135791235
1203561401203561402CT62GENIChomozygous144260819
1203561539203561540CT73GENIChomozygous144260820
1203561915203561916AG62GENIChomozygous144260821