chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25318958953189590CT23GENIChomozygous74716313
25319130153191302CA6GENIChomozygous78677212
25319175253191753CT25GENIChomozygous74716315
25319212853192129GT18GENIChomozygous74716317
25319253253192533TC31GENIChomozygous74716319
25319379853193799AT14GENIChomozygous74716321
25319426253194263AG23GENIChomozygous74716323
25319476653194767CT19GENIChomozygous74716325
25319511153195112GA26GENIChomozygous74716327
25319528153195282CT24GENIChomozygous74716329
25319575653195757CT17GENIChomozygous74716331
25319579653195797TA20GENIChomozygous74716333
25319612153196122GA17GENIChomozygous74716335
25319679853196799AG16GENIChomozygous74716337
25319698053196981CG17GENIChomozygous74716339
25319699753196998GA19GENIChomozygous74716341
25319733853197339AG8GENIChomozygous74716343
25319736353197364AG7GENIChomozygous74716345
25319743253197433TA12GENIChomozygous74716347
25321024553210246CT23GENIChomozygous74716353
25321026653210267TC18GENIChomozygous74716355
25321030053210301CA9GENICpossibly homozygous74716357
25321087953210880CT13GENIChomozygous74716359
25321118353211184TC5GENIChomozygous74716361
25321138253211383GC4GENIChomozygous74716363
25321141553211416GT5GENIChomozygous74716365
25321142153211422TC5GENIChomozygous74716367
25321154253211543TG7GENIChomozygous74716369
25321230753212308CT16GENIChomozygous74716373
25321381853213819GT16GENIChomozygous74716375
25321382553213826CT16GENIChomozygous74716377
25321453553214536TG20GENIChomozygous74716383
25321647053216471GA22GENIChomozygous74716385
25321747353217474AG20GENIChomozygous74716387
25321502053215021CT14GENIChomozygous75611782