chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131354253131354254TC18GENIChomozygous55722242
5131355340131355341TC26GENIChomozygous55722245
5131355578131355579CT23GENIChomozygous55722247
5131356145131356146CA11GENIChomozygous55722250
5131356462131356463GA21GENIChomozygous55722252
5131356529131356530TC27GENIChomozygous55722254
5131356762131356763CT26GENIChomozygous55722256
5131356859131356860CT30GENIChomozygous55722258
5131357053131357054GA19GENIChomozygous55722261
5131357237131357238AC32GENIChomozygous55722263
5131357371131357372TG23GENIChomozygous55722266
5131357636131357637GA9GENIChomozygous55722267
5131357913131357914CT17GENIChomozygous55722270
5131359368131359369CT14GENIChomozygous55722272
5131359898131359899AAC16GENIChomozygous55722274
5131359978131359979GA11GENIChomozygous55722277
5131360069131360070CT14GENICpossibly homozygous56531549
5131360097131360098CT19GENIChomozygous55722282
5131360378131360379GC6GENIChomozygous55722284
5131360385131360386C-6GENIChomozygous55722286
5131360425131360426AT5GENIChomozygous55722288
5131360443131360444CCT8GENIChomozygous55722291
5131360724131360725AG2GENIChomozygous55722293
5131360888131360889TC5GENIChomozygous55722296
5131360927131360930CCC---1GENIChomozygous55722298
5131363277131363278GT9GENIChomozygous55722301
5131365553131365554TC8GENIChomozygous55722303
5131367991131367992GA17GENIChomozygous55722313
5131367709131367710CT24GENIChomozygous56232051