chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8122004188122004189CG15GENIChomozygous116689764
8122039897122039898AT19GENIChomozygous116689766
8122029995122029995A25GENICheterozygous130673024
8122053371122053372AC10GENIChomozygous116988349
8122055397122055398GA7GENIChomozygous116689768
8122056046122056047GA17GENIChomozygous116689770
8122056102122056103TC21GENIChomozygous116689772
8122056118122056119TC19GENIChomozygous116689774
8122056147122056148T15GENIChomozygous128640219
8122057046122057047AG8GENIChomozygous116689776
8122059297122059299GT14GENICheterozygous128640221
8122062631122062631CTTTTTTCC12GENIChomozygous128640222
8122068148122068149T29GENIChomozygous128640225
8122055810122055810T12GENICheterozygous131694541
8122095743122095744CG5GENICheterozygous131891169
8122095745122095746CG3GENICheterozygous117149838
8122126673122126674CT26GENIChomozygous116689778
8122132577122132578GT36GENICheterozygous131061633
8122132587122132588GT34GENICheterozygous131061634
8122132589122132590AG33GENICheterozygous131061635
8122174255122174256GC14GENIChomozygous116689784
8122180542122180543CT27GENIChomozygous116689786