chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152996912152996913TC23GENIChomozygous112888968
4152999317152999318TC29GENIChomozygous112888969
4153000093153000094CT28GENIChomozygous113244927
4153000108153000109GA28GENIChomozygous113244928
4153000179153000180GA27GENIChomozygous113244929
4153000904153000905AG11GENIChomozygous113244930
4153001314153001315CT10GENIChomozygous113244931
4153002566153002567CG35GENICpossibly homozygous112888970
4153004150153004151GA4GENIChomozygous113244935
4153005014153005015AG29GENIChomozygous113244936
4153006082153006083CT17GENIChomozygous112888972
4153006764153006765CT26GENIChomozygous113244937
4153006791153006792TG32GENIChomozygous113244938
4153006975153006976GA38GENIChomozygous113244939
4153008551153008552CT24GENIChomozygous113244941
4153009773153009774TC21GENIChomozygous113244942
4153009841153009842AG20GENIChomozygous113244943
4153010203153010204GA23GENIChomozygous113244944
4153010694153010695TC23GENIChomozygous113244947
4153012014153012015TC21GENIChomozygous113244949
4153013387153013388TC23GENIChomozygous113244950
4153013629153013630GA26GENIChomozygous113244951
4153014533153014534AG23GENIChomozygous113244952
4153014834153014835TC28GENIChomozygous112888974
4153015879153015880TC21GENIChomozygous112888976
4153015987153015988CT22GENIChomozygous113244953
4153017055153017056AG24GENIChomozygous113244954