chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8123434664123434665CT14GENIChomozygous142107538
8123434857123434865ACAAACAG13GENIChomozygous142032287
8123435244123435244G14GENICpossibly homozygous142032288
8123436254123436255C16GENIChomozygous142032289
8123436612123436613GA26GENIChomozygous142107539
8123436719123436719G17GENIChomozygous142032290
8123436721123436721C18GENIChomozygous142032291
8123436722123436723GC17GENIChomozygous142107540
8123436724123436725AT18GENIChomozygous142107541
8123436834123436835CT25GENICpossibly homozygous142107542
8123436896123436897AG20GENIChomozygous142107543
8123437030123437031TC22GENIChomozygous142107544
8123437304123437304CCATATGTAACT20GENIChomozygous142032292
8123437706123437707GA15GENIChomozygous142107545
8123439503123439504TA12GENIChomozygous142107546