chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124383102124383103CT25GENIChomozygous54513655
7124383212124383213GA22GENIChomozygous54093497
7124383854124383855CT21GENIChomozygous54093499
7124386305124386306CT33GENIChomozygous54093501
7124386409124386410GGTTTTTTTTTTT12GENICheterozygous55097511
7124386423124386425GG--13GENICheterozygous55953248
7124386424124386425GGTTTTT13GENICheterozygous55953249
7124386748124386749CT8GENIChomozygous54093504
7124387379124387380CT28GENICpossibly homozygous54513657
7124388115124388116TG26GENIChomozygous54093506
7124388401124388402TC30GENIChomozygous54093508
7124388645124388646GA20GENIChomozygous54093510
7124389354124389355T-14GENIChomozygous54238087
7124389378124389379TTTTTCTTTTTTTTC8GENICpossibly homozygous55145081
7124389854124389855TG23GENIChomozygous54093516
7124389875124389876AG27GENICpossibly homozygous54513659
7124389942124389943CT31GENIChomozygous54513661
7124389972124389973AG26GENIChomozygous54513663
7124390195124390196TG39GENIChomozygous54093519
7124390296124390297CT29GENICpossibly homozygous54513665
7124390735124390736TG26GENIChomozygous54093525
7124391341124391342AG24GENIChomozygous54093529
7124391418124391419CT26GENIChomozygous54238089
7124391567124391568GC25GENIChomozygous54513667
7124392723124392724CT13GENIChomozygous54513671
7124392785124392786TG15GENIChomozygous54513673
7124392799124392800TC14GENIChomozygous54513675
7124393697124393698GA3GENIChomozygous54093537
7124394625124394626GA28GENIChomozygous54513677
7124394637124394638CG31GENIChomozygous54513679
7124395462124395463TC26GENIChomozygous54238135
7124395752124395753AG18GENIChomozygous54238141
7124396849124396850AG24GENIChomozygous54093547
7124397409124397410AG27GENIChomozygous54093549
7124398091124398092TC15GENIChomozygous54093551
7124398339124398340CA24GENIChomozygous54093553
7124398850124398851T-8GENIChomozygous54093555