chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141237931141237932GA25INTERGENIChomozygous54265436
7141238129141238130GC31INTERGENIChomozygous54158082
7141238771141238772AG28INTERGENIChomozygous54265439
7141239136141239137CT16INTERGENIChomozygous54158083
7141239820141239821A-38INTERGENIChomozygous54265442
7141240906141240907TC43GENICheterozygous54529523
7141240995141240996GA41GENICheterozygous54529525
7141241031141241032AG41GENICheterozygous54529527
7141241091141241092TC45GENICheterozygous54529529
7141241103141241104CT41GENICheterozygous54529531
7141241138141241139AG47GENICheterozygous54529533
7141241182141241183TC62GENICheterozygous54529535
7141241263141241264GA55GENICheterozygous54529543
7141241340141241341GA59GENICheterozygous54529545
7141241439141241440TG44GENICheterozygous54529547
7141241664141241665TC55GENICheterozygous54529549
7141241695141241696TC49GENICheterozygous54529551
7141241848141241849TC42GENICheterozygous54529553
7141241886141241887TC41GENICheterozygous54529555
7141241899141241900TC43GENICheterozygous54529557
7141241934141241935TC36GENICheterozygous54529559
7141241938141241939CCTT31GENICheterozygous54529561
7141242466141242467AACACCAC15INTERGENICpossibly homozygous54265445