chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137039086470390865GT58GENICheterozygous135215452
137039086770390868CA59GENICheterozygous135215453
137039087070390871CT58GENICheterozygous135215454
137039186970391870CG42GENIChomozygous135215455
137039289770392899TC27GENICheterozygous130585469
137047718870477190GT48GENICheterozygous133262485
137047982870479828T31GENIChomozygous129069448
137047983370479834GT31GENIChomozygous123758329
137047983570479835G30GENIChomozygous129069449
137047983870479838T30GENIChomozygous129069450
137047984770479847A25GENIChomozygous129069451
137047985470479854G23GENIChomozygous129069452
137047985670479857AG26GENIChomozygous123758334
137047987070479871AG23GENIChomozygous118459481
137047987670479876G20GENIChomozygous129069453
137047988170479881GGAG21GENIChomozygous129069454
137047989570479895G20GENIChomozygous129069455
137047990970479909G22GENIChomozygous129069456
137047991470479914GG22GENIChomozygous129069457
137047992170479921GG23GENIChomozygous129069458
137047992570479926AG22GENIChomozygous118459482
137047993670479936A23GENIChomozygous130418469
137048484670484846CC12GENIChomozygous130418470
137048488570484885CCC8GENIChomozygous129069465
137048488870484888CCC9GENIChomozygous129069466
137053308170533082G43GENIChomozygous129069508
137053314670533146G12GENIChomozygous129069509
137053318470533185G2GENIChomozygous129069510
137053338570533386CG2GENIChomozygous129111866
137053338770533388AC3GENIChomozygous129111867
137053352470533525G6GENIChomozygous129069512