chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117920930117920931GA18GENIChomozygous116672626
8117921471117921472GT53GENIChomozygous117920438
8117923231117923232TG52GENIChomozygous117920441
8117923566117923567TC45GENIChomozygous116672632
8117923661117923662GA43GENIChomozygous116672634
8117923869117923870TG43GENIChomozygous116672636
8117924081117924082CT26GENIChomozygous123049910
8117924094117924095CT25GENIChomozygous123049911
8117924500117924502CA29GENIChomozygous128636045
8117924632117924633AG32GENIChomozygous116672638
8117924728117924729GA37GENIChomozygous116672640
8117925148117925149TC37GENIChomozygous116672642
8117927690117927691CT55GENIChomozygous116887253
8117923713117923714CT49GENIChomozygous117969054
8117923801117923802GA43GENIChomozygous117969055
8117923986117923987CT31GENIChomozygous117969056
8117924509117924511GA29GENIChomozygous131054434
8117928102117928104CC43GENIChomozygous131054435
8117925751117925752CT44GENIChomozygous116887245
8117926305117926306AC58GENICpossibly homozygous116887249
8117927564117927565AG44GENIChomozygous116887251