chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45702021957020220TC13GENIChomozygous112657708
45702040057020401AC14GENIChomozygous112657709
45702080057020801GA18GENIChomozygous112657711
45702102857021029TC14GENIChomozygous112657712
45702113557021136CT12GENIChomozygous112657714
45702140557021406TC27GENIChomozygous112657715
45702204557022046GA24GENIChomozygous112657717
45702208457022085AG17GENIChomozygous112657719
45702224057022241CA23GENIChomozygous112657720
45702366057023661TC20GENICpossibly homozygous112657725
45702370457023705GA26GENIChomozygous112657727
45702448757024488CT22GENIChomozygous112657730
45702468857024689TC28GENIChomozygous112657731
45702488857024889CG6GENIChomozygous112657733
45702564557025646AG25GENIChomozygous112657734
45702612357026124TG28GENIChomozygous112657736
45702633757026338GA6GENIChomozygous112657738
45702712957027130TC14GENIChomozygous112657739
45702719857027199GC10GENIChomozygous112657741
45703080157030802GA6GENICheterozygous126014565
45703099057030991CT19GENIChomozygous112657746
45703485057034851TC18GENIChomozygous112657751
45703771957037720GA21GENIChomozygous112657752