chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135465924135465925TA10GENIChomozygous113386812
4135466418135466419AC7GENIChomozygous113386816
4135466667135466668TC7GENIChomozygous113386818
4135466772135466773GT10GENIChomozygous113386820
4135466907135466908TC10GENIChomozygous113386822
4135467006135467007GA4GENIChomozygous113386824
4135467032135467033AT5GENIChomozygous112837008
4135467071135467072AG9GENIChomozygous113386826
4135468099135468100AG10GENIChomozygous113386830
4135468362135468363GC11GENIChomozygous113386836
4135468511135468512TG11GENIChomozygous113386838
4135469761135469762TC8GENIChomozygous113386840
4135469848135469849AG7GENIChomozygous113386842
4135469902135469903GC8GENIChomozygous113386844
4135470013135470014GA9GENIChomozygous113386848