chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109721601497216015CG28GENIChomozygous116693171
109721641097216411AG23GENIChomozygous116693173
109722310997223110TC24GENIChomozygous116693175
109722329897223299CT26GENIChomozygous116693177
109722990797229908GA24GENIChomozygous116693179
109723070897230709AG37GENIChomozygous116693181
109723167097231671TC39GENIChomozygous116693183
109723291197232912CT11GENIChomozygous116693185
109723388997233890GA18GENIChomozygous116693187
109723652997236530CG25GENIChomozygous116693189
109723741797237418TC36GENICpossibly homozygous116693191