chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104632606346326064TTA10GENICheterozygous748159230
104632606346326064TTAA10GENICpossibly homozygous748159231
104632631846326319GA39GENIChomozygous635515262
104632646146326462CCAG22GENIChomozygous748159232
104632971746329718GA46GENIChomozygous635515263
104632979046329791AAGGTGGCTCAGC17GENIChomozygous748159233
104632994746329948A-19GENIChomozygous748159234
104633029746330298GT25GENIChomozygous635515264
104633285546332856GA50GENIChomozygous635515265
104633297346332974TG28GENIChomozygous635515266
104633378546333786AG37GENIChomozygous635515267
104633473446334757AGGATAGCCCACAGCAGGGCCAT-----------------------21GENIChomozygous748159235
104633479346334794TTTCACTCAC15GENIChomozygous748159237
104633540246335403AATG10GENICheterozygous748159238
104633540246335403AATGTG10GENICheterozygous748159239
104633576946335770TC34GENIChomozygous635515268
104633621146336227TCCGTCCGTCCGTCCG----------------1GENIChomozygous748159241
104633874846338749TTAC11GENICheterozygous748159244
104633874846338749TTACAC11GENICheterozygous748159245
104633874846338749TTACACAC11GENICheterozygous748159246
104633890346338904CT44GENIChomozygous635515269
104633948946339490AG40GENIChomozygous635515270
104633980546339806AT25GENIChomozygous635515271
104634082546340826CT34GENIChomozygous635515272
104634143546341436TC30GENIChomozygous635515273
104634327246343273GA22GENIChomozygous635515274
104634640946346410TC29GENIChomozygous635515275