chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141237931141237932GA26INTERGENIChomozygous54265436
7141238129141238130GC22INTERGENIChomozygous54158082
7141238771141238772AG21INTERGENIChomozygous54265439
7141239136141239137CT22INTERGENIChomozygous54158083
7141239820141239821A-17INTERGENIChomozygous54265442
7141240906141240907TC35GENICheterozygous54529523
7141240995141240996GA41GENICheterozygous54529525
7141241031141241032AG45GENICheterozygous54529527
7141241091141241092TC42GENICheterozygous54529529
7141241103141241104CT39GENICheterozygous54529531
7141241138141241139AG35GENICheterozygous54529533
7141241182141241183TC40GENICheterozygous54529535
7141241230141241231TC33GENICheterozygous54529537
7141241232141241233TC34GENICheterozygous54529539
7141241240141241241GA34GENICheterozygous54529541
7141241263141241264GA32GENICheterozygous54529543
7141241340141241341GA29GENICheterozygous54529545
7141241439141241440TG39GENICheterozygous54529547
7141241664141241665TC36GENICheterozygous54529549
7141241695141241696TC30GENICheterozygous54529551
7141241848141241849TC42GENICheterozygous54529553
7141241886141241887TC35GENICheterozygous54529555
7141241899141241900TC35GENICheterozygous54529557
7141241934141241935TC32GENICheterozygous54529559
7141241938141241939CCTT19GENICheterozygous54529561
7141242466141242467AACACCAC8INTERGENIChomozygous54265445