chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71302412813024129CA23GENIChomozygous53792468
71302497613024977A-14GENICheterozygous54301910
71302499313024994CCAAAA15GENIChomozygous53792469
71302601713026018CT18GENIChomozygous53792471
71302712313027124TC22GENIChomozygous53792474
71302955713029558GA25GENIChomozygous53792475
71303144613031449CCC---9GENIChomozygous53792476
71303162413031625CT17GENIChomozygous53792477
71303323213033233TC16GENIChomozygous53792478
71303348113033482TC18GENIChomozygous53792479
71303570413035705CCTTGGAGCAGT26GENIChomozygous53792480
71303634613036347CG29GENIChomozygous53792482
71303675313036754TC37GENIChomozygous53792483
71303714913037150AG24GENIChomozygous53792484
71303737213037373AG25GENIChomozygous53792485
71303769713037698AATG22GENICpossibly homozygous53792486
71303919013039191TC16GENIChomozygous53792487
71304128713041288AACC5GENICheterozygous53792488
71304128713041288AAC5GENICheterozygous53792489
71304169913041700GGA26GENIChomozygous53792490
71304224413042245TC28GENIChomozygous53792491
71304252813042529AACCT23GENIChomozygous53792492
71304285613042857TC27GENIChomozygous53792493
71304305113043052CA22GENIChomozygous53792494
71304342113043422CT34GENIChomozygous53792495
71304369613043697AG18GENIChomozygous53792496
71304592613045927CT16GENIChomozygous53792497
71304735213047353CT19GENIChomozygous53792498
71305077413050775TC23GENIChomozygous53792499
71305087113050872TC28GENIChomozygous53792500
71305131413051315GA16GENIChomozygous53792501
71302627313026287CACACACACACACA--------------14GENICheterozygous54955183
71302627513026287CACACACACACA------------14GENICheterozygous54955185
71302752013027521GGA13GENICheterozygous54955187
71302752013027521GGAAA13GENICheterozygous55057510