chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2033109383310939TG19GENIChomozygous109370704
2033109813310982AG27GENIChomozygous109068414
2033114233311424AT27GENIChomozygous109370706
2033121293312130CT30GENIChomozygous109370709
2033126813312682GA28GENIChomozygous109370711
2033141813314182TC18GENIChomozygous109068422
2033148723314873CT33GENIChomozygous109068426
2033149633314964GA21GENIChomozygous109068428
2033151253315126GA17GENIChomozygous109068430
2033151663315167CT26GENIChomozygous109068432
2033153943315395CA14GENIChomozygous109068440
2033153963315397AG14GENIChomozygous109068442
2033156813315682GA19GENIChomozygous109370715
2033162123316213CA24GENIChomozygous109068446
2033170963317097GC40GENIChomozygous109068450
2033171583317159GC36GENIChomozygous109068452
2033173433317344CT31GENIChomozygous109388924
2033176943317695TC33GENIChomozygous109068454
2033179803317981TC39GENIChomozygous109068456
2033188023318803AG23GENIChomozygous109068458
2033203253320326CT22GENIChomozygous109388925
2033212873321288GA21GENIChomozygous109068460
2033213753321376CT14GENIChomozygous109068462
2033217633321764GT20GENIChomozygous109388926
2033220533322054AT23GENIChomozygous109068464