chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101239506612395067GA45GENICpossibly homozygous52028628
101239605212396053GA59GENIChomozygous51618734
101239615012396151GC58GENIChomozygous52028630
101239676312396764TG49GENIChomozygous52028632
101239717312397174CA49GENIChomozygous52028634
101239717512397176GA50GENIChomozygous52028636
101239736912397370TG49GENIChomozygous52028638
101239759712397601ACAC----10GENICpossibly homozygous51806756
101239759912397601AC--10GENICheterozygous51806758
101239836712398385TGTATGTGTACACGTGTG------------------31GENIChomozygous51327740