chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116730602116730603CT18INTERGENIChomozygous53291273
8116730989116730990CCCTTT12INTERGENIChomozygous53291275
8116731185116731186AG22INTERGENIChomozygous53291276
8116731395116731396TC17INTERGENIChomozygous53291277
8116732077116732078GA37GENIChomozygous53291278
8116734622116734623TTC15GENIChomozygous53721468
8116734979116734980GGT8GENICheterozygous52828606
8116734979116734980GGTT8GENICheterozygous52828607
8116734979116734980GGTTT8GENICheterozygous53471861
8116737670116737671AC29GENIChomozygous53291279
8116737752116737753TC35GENIChomozygous53291280
8116738646116738647AG32GENIChomozygous53291281
8116738965116738966GGC5GENICheterozygous53368018
8116739404116739408TTTT----8GENIChomozygous53183457
8116740060116740061AG23GENIChomozygous53291282
8116740142116740143TTAA9GENICheterozygous53471863
8116740143116740145AA--9GENICpossibly homozygous53183458
8116740295116740296CA19GENIChomozygous52828610
8116740619116740620GGA6GENICheterozygous53291283
8116740646116740650GTGA----2GENIChomozygous53291284
8116741509116741510A-31GENIChomozygous53291285
8116742479116742480AT17GENIChomozygous53291286
8116742981116742982TC19GENIChomozygous53291287
8116743134116743143AAAAAAAAC---------6GENICheterozygous53523642
8116743135116743143AAAAAAAC--------6GENICheterozygous53721470
8116743160116743161AC14GENIChomozygous53721472
8116743178116743179CT20GENIChomozygous53291288
8116743245116743246GA24GENIChomozygous53291289
8116743546116743547GA29GENIChomozygous53291290
8116744759116744760AG19GENIChomozygous53291291
8116746423116746427AAAA----14GENIChomozygous53291292
8116746506116746507CA28GENIChomozygous53291294
8116748629116748630CCA16GENIChomozygous53291295
8116748668116748669CCAAAAAAAAAAAA14GENIChomozygous53454636