chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147717800147717801GA23GENIChomozygous114047014
5147723343147723344GA42GENIChomozygous114047016
5147723732147723733AT12GENIChomozygous114047018
5147723749147723750CT11GENIChomozygous114047020
5147724691147724692GA33GENIChomozygous114047024
5147726247147726248GA18GENIChomozygous114047026
5147727067147727068TC34GENIChomozygous114047028
5147727669147727670CG23GENIChomozygous114047032
5147728259147728260AG9GENICpossibly homozygous114047034
5147728918147728919AG23GENIChomozygous114047036
5147733074147733075CT31GENIChomozygous114047038
5147734121147734122TC25GENIChomozygous114047040
5147734261147734262GA24GENIChomozygous114047042
5147735322147735323TC12GENIChomozygous114047044
5147736582147736583AT28GENIChomozygous114047046
5147738756147738757TA44GENIChomozygous114047050
5147740877147740878AG14GENIChomozygous114047052
5147740993147740994AC20GENIChomozygous114047054
5147741912147741913GA12GENIChomozygous114047060
5147742438147742439GA21GENIChomozygous114047062
5147742484147742485CA12GENIChomozygous114047064