chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102939056529390566GC27GENIChomozygous116540171
102939058829390589GA25GENIChomozygous116540173
102939090329390904AG21GENIChomozygous116540175
102939124929391250CT25GENIChomozygous116540177
102939154829391549TC18GENIChomozygous116540179
102939168729391688GT18GENIChomozygous116540181
102939185829391859AC24GENIChomozygous116540183
102939193129391932CT36GENIChomozygous116540185
102939199629391997AG35GENICpossibly homozygous116540187
102939249229392493GA14GENIChomozygous116751159