chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104632606346326064TTA11GENICheterozygous743052816
104632606346326064TTAA11GENICpossibly homozygous743052817
104632631846326319GA11GENIChomozygous626096182
104632646146326462CCAG25GENIChomozygous743052818
104632971746329718GA22GENIChomozygous626096183
104632979046329791AAGGTGGCTCAGC18GENIChomozygous743052819
104632994746329948A-21GENIChomozygous743052820
104633029746330298GT31GENIChomozygous626096184
104633285546332856GA30GENIChomozygous626096185
104633297346332974TG26GENIChomozygous626096186
104633378546333786AG15GENIChomozygous626096187
104633473446334757AGGATAGCCCACAGCAGGGCCAT-----------------------17GENIChomozygous743052821
104633479346334794TTTCAC9GENIChomozygous743052822
104633540246335403AATG5GENICheterozygous743052824
104633540246335403AATGTG5GENICheterozygous743052825
104633540246335403AATGTGTG5GENICheterozygous743052826
104633576946335770TC23GENIChomozygous626096188
104633874846338749TTAC3GENICheterozygous743052827
104633874846338749TTACACAC3GENICheterozygous743052829
104633890346338904CT27GENIChomozygous626096189
104633948946339490AG21GENIChomozygous626096190
104633980546339806AT19GENIChomozygous626096191
104634082546340826CT29GENIChomozygous626096192
104634143546341436TC17GENIChomozygous626096193
104634327246343273GA8GENICpossibly homozygous626096194
104634640946346410TC21GENIChomozygous626096195