chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104632606346326064TTA18GENICheterozygous757090361
104632631846326319GA16GENIChomozygous649971934
104632646146326462CCAG25GENIChomozygous757090363
104632675746326758AG16GENIChomozygous649971935
104632725246327253TC19GENIChomozygous649971936
104632971746329718GA15GENIChomozygous649971937
104632979046329791AAGGTGGCTCAGC9GENIChomozygous757090364
104632994746329948A-11GENICpossibly homozygous757090365
104632999446329995CT16GENIChomozygous649971938
104633285546332856GA14GENICpossibly homozygous649971939
104633297346332974TG14GENIChomozygous649971940
104633378546333786AG19GENIChomozygous649971941
104633479346334794TTTCAC3GENIChomozygous757090366
104633523946335240AT27GENIChomozygous649971942
104633569446335695AT22GENIChomozygous649971943
104633576946335770TC20GENIChomozygous649971944
104633621146336227TCCGTCCGTCCGTCCG----------------9GENIChomozygous757090368
104633687346336874CT27GENIChomozygous649971945
104633890346338904CT23GENIChomozygous649971946
104633948946339490AG15GENIChomozygous649971947
104633980546339806AT26GENIChomozygous649971948
104634130346341304CT21GENIChomozygous649971949
104634143546341436TC21GENIChomozygous649971950
104634267846342679GA28GENIChomozygous649971951
104634327246343273GA25GENIChomozygous649971952
104634360446343605GA20GENIChomozygous649971953
104634472346344724GT15GENICheterozygous649971954
104634670046346701AC25GENIChomozygous649971955
104634722346347224GA21GENIChomozygous649971956
104634778546347797CAAGTTCCTGGC------------8GENIChomozygous757090371
104634783946347840AG13GENIChomozygous649971957