chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141237931141237932GA16INTERGENIChomozygous54265436
7141238129141238130GC10INTERGENIChomozygous54158082
7141238771141238772AG12INTERGENIChomozygous54265439
7141239136141239137CT21INTERGENIChomozygous54158083
7141239820141239821A-17INTERGENIChomozygous54265442
7141240995141240996GA28GENICheterozygous54529525
7141241031141241032AG26GENICheterozygous54529527
7141241091141241092TC23GENICheterozygous54529529
7141241103141241104CT21GENICheterozygous54529531
7141241263141241264GA15GENICheterozygous54529543
7141241340141241341GA31GENICheterozygous54529545
7141241439141241440TG19GENICheterozygous54529547
7141241664141241665TC27GENICheterozygous54529549
7141241695141241696TC20GENICheterozygous54529551
7141241848141241849TC19GENICheterozygous54529553
7141241886141241887TC19GENICheterozygous54529555
7141241899141241900TC23GENICheterozygous54529557
7141241934141241935TC22GENICheterozygous54529559
7141241938141241939CCTT24GENICheterozygous54529561
7141242134141242135GT17GENICheterozygous56444436
7141242146141242147CT16GENICheterozygous56444438