chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124382451124382453CC--6GENIChomozygous54093493
7124382686124382687AATT25GENICpossibly homozygous54093495
7124382686124382687AAT25GENICheterozygous55097509
7124383212124383213GA10GENIChomozygous54093497
7124383854124383855CT9GENIChomozygous54093499
7124384713124384714GGGGTGT1GENIChomozygous55003734
7124386305124386306CT10GENIChomozygous54093501
7124386409124386410GGTTTTTTTTTTT3GENIChomozygous55097511
7124386748124386749CT10GENIChomozygous54093504
7124388115124388116TG13GENIChomozygous54093506
7124388401124388402TC10GENIChomozygous54093508
7124388645124388646GA11GENIChomozygous54093510
7124389372124389373CCTTTTTTTTTTTTTTTTTT4GENIChomozygous55059772
7124389535124389536GA19GENIChomozygous54093512
7124389691124389692TTAA12GENIChomozygous54093514
7124389854124389855TG11GENIChomozygous54093516
7124389865124389866TC13GENIChomozygous54093517
7124390195124390196TG5GENIChomozygous54093519
7124390205124390206CT4GENIChomozygous54093521
7124390532124390533GT7GENIChomozygous54093523
7124390735124390736TG18GENIChomozygous54093525
7124390916124390917GA10GENIChomozygous54093527
7124391341124391342AG6GENIChomozygous54093529
7124391650124391651GGCACACACA2GENIChomozygous55097515
7124392722124392723TTCC1GENIChomozygous54093535
7124393697124393698GA18GENIChomozygous54093537
7124394073124394074TTA10GENIChomozygous54093541
7124394696124394697CT22GENIChomozygous54093543
7124394727124394728CT19GENIChomozygous54093545
7124396849124396850AG18GENIChomozygous54093547
7124397409124397410AG18GENIChomozygous54093549
7124398091124398092TC11GENIChomozygous54093551
7124398339124398340CA7GENIChomozygous54093553
7124398850124398851T-5GENIChomozygous54093555