chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104632606346326064TTA20GENICheterozygous736146377
104632606346326064TTAA20GENICpossibly homozygous736146378
104632631846326319GA37GENIChomozygous614015296
104632646146326462CCAG34GENIChomozygous736146379
104632971746329718GA31GENIChomozygous614015297
104632979046329791AAGGTGGCTCAGC25GENIChomozygous736146380
104632994746329948A-11GENIChomozygous736146381
104633029746330298GT33GENIChomozygous615969647
104633285546332856GA26GENIChomozygous614015298
104633297346332974TG44GENIChomozygous614015299
104633378546333786AG26GENIChomozygous614015300
104633473446334757AGGATAGCCCACAGCAGGGCCAT-----------------------7GENIChomozygous736146382
104633479346334794TTTCACTCAC7GENIChomozygous736146384
104633576946335770TC27GENIChomozygous614015301
104633621146336227TCCGTCCGTCCGTCCG----------------1GENIChomozygous736146385
104633890346338904CT28GENIChomozygous614015302
104633948946339490AG32GENIChomozygous614015303
104633980546339806AT23GENIChomozygous614015304
104634082546340826CT32GENIChomozygous615969648
104634143546341436TC24GENIChomozygous614015305
104634327246343273GA25GENIChomozygous614015306
104634640946346410TC18GENIChomozygous615969649