chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71302412813024129CA28GENIChomozygous53792468
71302499313024994CCAAAA7GENIChomozygous53792469
71302601713026018CT14GENIChomozygous53792471
71302627313026287CACACACACACACA--------------19GENICheterozygous54955183
71302627513026287CACACACACACA------------19GENICheterozygous54955185
71302712313027124TC27GENIChomozygous53792474
71302752013027521GGA9GENICpossibly homozygous54955187
71302955713029558GA27GENIChomozygous53792475
71303144613031449CCC---14GENIChomozygous53792476
71303162413031625CT21GENIChomozygous53792477
71303323213033233TC13GENIChomozygous53792478
71303348113033482TC32GENIChomozygous53792479
71303570413035705CCTTGGAGCAGT33GENIChomozygous53792480
71303634613036347CG24GENIChomozygous53792482
71303675313036754TC21GENIChomozygous53792483
71303714913037150AG22GENIChomozygous53792484
71303737213037373AG32GENIChomozygous53792485
71303769713037698AATG17GENICpossibly homozygous53792486
71303919013039191TC11GENIChomozygous53792487
71304128713041288AACC4GENIChomozygous53792488
71304169913041700GGA18GENIChomozygous53792490
71304224413042245TC27GENIChomozygous53792491
71304252813042529AACCT20GENIChomozygous53792492
71304285613042857TC22GENIChomozygous53792493
71304305113043052CA22GENIChomozygous53792494
71304342113043422CT22GENIChomozygous53792495
71304369613043697AG30GENIChomozygous53792496
71304592613045927CT35GENIChomozygous53792497
71304735213047353CT28GENIChomozygous53792498
71305077413050775TC14GENIChomozygous53792499
71305087113050872TC23GENIChomozygous53792500
71305131413051315GA17GENIChomozygous53792501