chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101239506612395067GA17GENIChomozygous52028628
101239615012396151GC8GENIChomozygous52028630
101239676312396764TG11GENICpossibly homozygous52028632
101239717312397174CA11GENIChomozygous52028634
101239717512397176GA10GENIChomozygous52028636
101239736912397370TG16GENIChomozygous52028638
101239605212396053GA25GENIChomozygous51618734
101239836712398385TGTATGTGTACACGTGTG------------------5GENIChomozygous51327740