chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71105449911054500TC26GENIChomozygous115567900
71105517111055172GA19GENIChomozygous115567901
71105612411056125CA15GENIChomozygous115567902
71105696611056967AG25GENIChomozygous115567903
71105745211057453AG18GENICpossibly homozygous115567904
71105893611058937AT20GENIChomozygous115567907
71105984711059848GC32GENIChomozygous115567908
71106020911060210GT28GENIChomozygous115567909
71106024511060246TC22GENIChomozygous115567910
71106028911060290GA27GENIChomozygous115567911
71106029011060291CA29GENIChomozygous115567912
71106037111060372CA25GENIChomozygous115567913
71106103611061037AG25GENIChomozygous115567914
71106107211061073GA27GENIChomozygous115567915
71106123211061233GT29GENIChomozygous115567916
71106132411061325AG35GENIChomozygous115567917
71106918611069187CT33GENIChomozygous115567918
71107263211072633TG16GENIChomozygous115567924
71107426111074262AG33GENIChomozygous115567925
71107494911074950TA24GENIChomozygous115567926
71107510811075109GA24GENIChomozygous115567927