chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143413016143413017GA45GENIChomozygous118323962
7143413137143413138AC40GENICpossibly homozygous118323964
7143413595143413596TC44GENIChomozygous118323966
7143413805143413806CT41GENIChomozygous118323968
7143413894143413895GA37GENIChomozygous118323970
7143413951143413952TC39GENIChomozygous118323972
7143413961143413962TC39GENIChomozygous116099796
7143414059143414060TC48GENIChomozygous118323974
7143414524143414525CT40GENIChomozygous118323976
7143414799143414800AG34GENIChomozygous118323978
7143414859143414860CA33GENIChomozygous118323980
7143415136143415137TC30GENIChomozygous118323982
7143415198143415199AG37GENIChomozygous118323984
7143415517143415518TG39GENIChomozygous118323986
7143415579143415605AGACAGAGAGACACACACAGAGAGAC33GENIChomozygous131435540
7143416216143416217GA37GENIChomozygous118323988
7143416616143416617GA39GENIChomozygous118323990
7143416967143416968CT36GENIChomozygous118323992
7143417928143417929CT15GENIChomozygous118323994
7143418643143418644CT45GENIChomozygous118323996
7143420182143420183CG53GENIChomozygous118323998
7143417984143417985CA24GENIChomozygous115943790
7143416551143416552AG44GENIChomozygous115943789