chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31721332817213329GA16GENIChomozygous112075649
31721397117213972TC28GENIChomozygous112075653
31721399917214000GT14GENIChomozygous112075655
31721412917214130AG16GENIChomozygous112075657
31721414217214143AT16GENIChomozygous112075659
31721416217214163GA13GENIChomozygous112075661
31721448617214487GA13GENIChomozygous112075663
31721561017215611AC10GENIChomozygous111884227
31721571617215717GA17GENIChomozygous112411932
31721591617215917AT19GENIChomozygous112075665
31721593717215938CT11GENIChomozygous112075667
31721608517216086CG6GENIChomozygous112075669
31721620017216201AG20GENIChomozygous112075671
31721668317216684CT30GENICheterozygous112075673
31721686517216866CG5GENIChomozygous112075675
31721687617216877AG5GENIChomozygous112075677
31721692617216927GC5GENIChomozygous112075679
31721759517217596AG31GENIChomozygous112075683