chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118526357118526358GC13GENIChomozygous967335714
8118527316118527317AC22GENIChomozygous967335715
8118527665118527666CT15GENIChomozygous967335716
8118527743118527744TC15GENIChomozygous967335717
8118528101118528102CG22GENIChomozygous967335718
8118528291118528292CT23GENIChomozygous967335719
8118528481118528482GA29GENIChomozygous967335720
8118529024118529025AC28GENICpossibly homozygous967335721
8118529158118529159AG21GENIChomozygous967335722
8118529188118529189AG19GENICpossibly homozygous967335723
8118529280118529281AG25GENIChomozygous967335724
8118529731118529732CA21GENIChomozygous967335725
8118530004118530005CA19GENICpossibly homozygous967335726
8118530694118530695TG30GENICpossibly homozygous967335727
8118531195118531196TG23GENICpossibly homozygous967335728
8118532000118532001CT24GENIChomozygous967335729
8118532272118532273CG19GENIChomozygous967335730
8118533158118533159GA26GENIChomozygous967335731
8118534045118534046TC18GENIChomozygous967335732
8118534207118534208TC26GENIChomozygous967335733
8118534298118534299TC22GENIChomozygous967335734
8118536456118536457TA15GENIChomozygous967335735
8118538916118538917CT16GENIChomozygous967335736
8118539595118539596GA26GENIChomozygous967335737
8118539596118539597AT26GENIChomozygous967335738
8118540242118540243GT23GENIChomozygous967335739