chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113413664034136641TA18GENIChomozygous116036503
113413848534138486CT21GENIChomozygous116099141
113413910234139103CT11GENICpossibly homozygous116099143
113413996534139966CA24GENICpossibly homozygous116099145
113414046734140468TC35GENICpossibly homozygous116099147
113414086734140868TC29GENIChomozygous115819637
113414130834141309CT23GENIChomozygous116099149
113414176734141768GA22GENIChomozygous115819639
113414178134141782TC20GENIChomozygous115819641
113414197034141971GT22GENIChomozygous116099151
113414213434142135CT19GENIChomozygous115819643
113414220134142202CT31GENIChomozygous116099153
113414248434142485GC27GENICpossibly homozygous115819645
113414249434142495GA25GENICpossibly homozygous116099155