chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141238004141238005TA32INTERGENIChomozygous54678416
7141238129141238130GC45INTERGENIChomozygous54158082
7141238771141238772AG40INTERGENICpossibly homozygous54265439
7141239136141239137CT38INTERGENIChomozygous54158083
7141239637141239638CT32INTERGENIChomozygous54678418
7141239820141239821A-37INTERGENIChomozygous54265442
7141240883141240884CT29GENICpossibly homozygous54678420
7141240906141240907TC34GENICheterozygous54529523
7141240995141240996GA54GENICheterozygous54529525
7141241031141241032AG49GENICheterozygous54529527
7141241091141241092TC44GENICheterozygous54529529
7141241103141241104CT43GENICheterozygous54529531
7141241138141241139AG48GENICheterozygous54529533
7141241182141241183TC37GENICheterozygous54529535
7141241230141241231TC36GENICheterozygous54529537
7141241232141241233TC35GENICheterozygous54529539
7141241240141241241GA39GENICheterozygous54529541
7141241263141241264GA48GENICheterozygous54529543
7141241340141241341GA62GENICheterozygous54529545
7141241439141241440TG76GENICheterozygous54529547
7141241664141241665TC45GENICheterozygous54529549
7141241695141241696TC55GENICheterozygous54529551
7141241848141241849TC51GENICheterozygous54529553
7141241886141241887TC45GENICheterozygous54529555
7141241899141241900TC49GENICheterozygous54529557
7141241934141241935TC45GENICheterozygous54529559
7141241938141241939CCTT38GENICheterozygous54529561
7141242230141242231A-35GENICheterozygous54158088
7141242467141242470CAC---3INTERGENIChomozygous54158090