chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101239506612395067GA21GENIChomozygous52028628
101239615012396151GC4GENIChomozygous52028630
101239676312396764TG16GENICpossibly homozygous52028632
101239717312397174CA9GENIChomozygous52028634
101239717512397176GA9GENIChomozygous52028636
101239736912397370TG18GENIChomozygous52028638
101239605212396053GA19GENICpossibly homozygous51618734
101239836712398385TGTATGTGTACACGTGTG------------------5GENIChomozygous51327740