chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131354253131354254TC10GENIChomozygous55722242
5131355340131355341TC10GENIChomozygous55722245
5131355578131355579CT18GENIChomozygous55722247
5131356145131356146CA13GENIChomozygous55722250
5131356462131356463GA12GENIChomozygous55722252
5131356529131356530TC15GENIChomozygous55722254
5131356762131356763CT13GENIChomozygous55722256
5131356859131356860CT5GENIChomozygous55722258
5131357053131357054GA12GENIChomozygous55722261
5131357237131357238AC9GENIChomozygous55722263
5131357371131357372TG9GENIChomozygous55722266
5131357636131357637GA11GENIChomozygous55722267
5131357913131357914CT13GENIChomozygous55722270
5131359368131359369CT2GENIChomozygous55722272
5131359898131359899AAC7GENIChomozygous55722274
5131359978131359979GA11GENIChomozygous55722277
5131360037131360038CCGTAT5GENICheterozygous56645664
5131360069131360070CT6GENIChomozygous56531549
5131360097131360098CT9GENIChomozygous55722282
5131360378131360379GC6GENIChomozygous55722284
5131360385131360386C-5GENIChomozygous55722286
5131360425131360426AT3GENIChomozygous55722288
5131360443131360444CCT3GENIChomozygous55722291
5131360724131360725AG5GENIChomozygous55722293
5131360888131360889TC5GENIChomozygous55722296
5131360927131360930CCC---2GENIChomozygous55722298
5131363277131363278GT6GENIChomozygous55722301
5131363832131363833GGA11GENICheterozygous56493441
5131365553131365554TC2GENIChomozygous55722303
5131367709131367710CT12GENIChomozygous56232051
5131367991131367992GA11GENIChomozygous55722313