chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5118666328118666329G-42GENIChomozygous707084958
5118667069118667070C-29GENICpossibly homozygous707084959
5118671033118671034TC54GENIChomozygous559149860
5118671684118671685GA28GENIChomozygous559149861
5118672285118672286CT20GENIChomozygous559149862
5118673218118673219GA20GENIChomozygous559149863
5118675465118675466CA25GENIChomozygous559149864
5118675836118675837CA23GENIChomozygous559149865
5118677185118677186CCT13GENIChomozygous707084960
5118677255118677256GT11GENIChomozygous561009779
5118677282118677283CCAT4GENIChomozygous707084961
5118677327118677328TC10GENIChomozygous561009780
5118678871118678881CACACACACA----------16GENICheterozygous707084962
5118678873118678881CACACACA--------16GENICpossibly homozygous707084963
5118679190118679191CA19GENIChomozygous561009781
5118679194118679195CA18GENIChomozygous561009782
5118679196118679197CA19GENIChomozygous561009783
5118679198118679199CA19GENIChomozygous561009784
5118679200118679201CA19GENIChomozygous561009785
5118679307118679308C-19GENIChomozygous707084966
5118679329118679330CA19GENIChomozygous561009786