chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121351511121351512AC5GENIChomozygous889723350
7121351659121351660AG13GENIChomozygous889723351
7121351666121351667GA17GENIChomozygous889723352
7121352112121352113AG18GENIChomozygous889723353
7121352821121352822AG6GENIChomozygous889723354
7121354407121354408AG10GENIChomozygous889723355
7121354414121354415CT9GENIChomozygous889723356
7121354892121354893AC15GENIChomozygous889723357
7121355445121355446TA6GENIChomozygous889723358
7121357005121357006TG18GENIChomozygous889723359
7121364820121364821CT14GENIChomozygous889723365
7121365669121365670TC17GENIChomozygous889723366
7121367352121367353TC20GENIChomozygous889723367
7121367375121367376GA22GENIChomozygous889723368
7121369373121369374AG17GENIChomozygous889723369
7121370431121370432TC20GENIChomozygous889723370
7121370678121370679CT26GENIChomozygous889723371
7121371103121371104GA12GENIChomozygous889723372
7121372869121372870TC19GENIChomozygous889723373
7121373043121373044TC26GENICpossibly homozygous889723374
7121374131121374132AG22GENIChomozygous889723375
7121374767121374768CT6GENIChomozygous889723376
7121376233121376234TC21GENIChomozygous889723377
7121377740121377741CT22GENIChomozygous889723378
7121378332121378333TC33GENICpossibly homozygous889723379
7121379448121379449GA17GENIChomozygous889723380
7121380634121380635TC18GENIChomozygous889723381
7121382028121382029GA18GENIChomozygous889723382