chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71302412813024129CA41GENIChomozygous53792468
71302499313024994CCAAAA14GENICpossibly homozygous53792469
71302499313024994CCAAA14GENICheterozygous53792470
71302601713026018CT22GENIChomozygous53792471
71302627313026287CACACACACACACA--------------18GENICheterozygous54955183
71302627513026287CACACACACACA------------18GENICheterozygous54955185
71302712313027124TC41GENIChomozygous53792474
71302752013027521GGA17GENICheterozygous54955187
71302955713029558GA25GENIChomozygous53792475
71303144613031449CCC---14GENIChomozygous53792476
71303162413031625CT19GENIChomozygous53792477
71303323213033233TC24GENIChomozygous53792478
71303348113033482TC18GENIChomozygous53792479
71303570413035705CCTTGGAGCAGT28GENIChomozygous53792480
71303634613036347CG25GENIChomozygous53792482
71303675313036754TC31GENIChomozygous53792483
71303714913037150AG24GENIChomozygous53792484
71303717013037171C-19GENICheterozygous55391593
71303737213037373AG19GENIChomozygous53792485
71303769713037698AATG16GENICheterozygous53792486
71303769713037698AATGTG16GENICpossibly homozygous54558171
71303919013039191TC29GENIChomozygous53792487
71304128713041288AACC23GENICpossibly homozygous53792488
71304128713041288AAC23GENICheterozygous53792489
71304169913041700GGA32GENIChomozygous53792490
71304224413042245TC25GENIChomozygous53792491
71304252813042529AACCT27GENIChomozygous53792492
71304285613042857TC23GENIChomozygous53792493
71304305113043052CA30GENIChomozygous53792494
71304342113043422CT30GENIChomozygous53792495
71304369613043697AG24GENIChomozygous53792496
71304592613045927CT38GENIChomozygous53792497
71304735213047353CT39GENIChomozygous53792498
71305077413050775TC15GENIChomozygous53792499
71305087113050872TC19GENIChomozygous53792500
71305131413051315GA23GENIChomozygous53792501