chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101120697311206974CG7GENIChomozygous116734323
101120833211208333GA40GENIChomozygous116734325
101121134111211342TG7GENICheterozygous117176902
101121186711211868CT31GENIChomozygous116734326
101121400111214002AG35GENIChomozygous116734327
101121572311215724CT18GENIChomozygous116734328
101121630511216306TC21GENIChomozygous116734329
101121842011218421GT22GENICpossibly homozygous116734330
101121842411218425CG22GENICpossibly homozygous116734331
101122197711221978TC18GENIChomozygous116858955