chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87640088076400881AG23GENIChomozygous116969454
87640213476402135GA38GENIChomozygous116969455
87640378276403783AG23GENIChomozygous116969456
87640385176403852CT29GENIChomozygous116969457
87640445676404457AC17GENIChomozygous116969458
87640682876406829CT5GENIChomozygous116969459
87640685476406855CT8GENICheterozygous116844425
87640912276409123GA27GENIChomozygous116969460
87640913776409138AG21GENIChomozygous116969461
87640942676409427TC23GENIChomozygous116969462
87640993876409939GA20GENIChomozygous116969463
87641218376412184CG24GENIChomozygous116969464
87641286076412861AG18GENIChomozygous116969465
87641531976415320AG29GENIChomozygous116969466
87641623576416236TC34GENIChomozygous116969467
87641793476417935GA29GENICpossibly homozygous116969468
87641825476418255CT34GENICpossibly homozygous116969469
87641911476419115TC17GENIChomozygous116969470
87642095476420955CT17GENIChomozygous116969471
87642102776421028AG18GENIChomozygous116969472
87642347776423478CT21GENIChomozygous116969473
87642382676423827AT29GENIChomozygous116969474
87642404876424049GA32GENIChomozygous116969475
87642546476425465CT32GENIChomozygous116969476
87642565476425655CT21GENIChomozygous116969477