chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25318958953189590CT27GENIChomozygous74716313
25319175253191753CT28GENIChomozygous74716315
25319212853192129GT27GENIChomozygous74716317
25319253253192533TC22GENIChomozygous74716319
25319130153191302CA6GENIChomozygous78677212
25319379853193799AT17GENIChomozygous74716321
25319426253194263AG21GENIChomozygous74716323
25319476653194767CT25GENIChomozygous74716325
25319511153195112GA23GENICpossibly homozygous74716327
25319528153195282CT23GENIChomozygous74716329
25319575653195757CT24GENIChomozygous74716331
25319579653195797TA31GENIChomozygous74716333
25319612153196122GA19GENIChomozygous74716335
25319679853196799AG9GENIChomozygous74716337
25319698053196981CG25GENIChomozygous74716339
25319699753196998GA28GENIChomozygous74716341
25319733853197339AG19GENIChomozygous74716343
25321030053210301CA12GENICheterozygous74716357
25319736353197364AG14GENIChomozygous74716345
25319743253197433TA9GENIChomozygous74716347
25319998953199990GC5GENIChomozygous74716351
25321024553210246CT21GENIChomozygous74716353
25321026653210267TC15GENIChomozygous74716355
25320024453200245GA18GENICheterozygous73604002
25321000153210002CA4GENICheterozygous73604006
25321087953210880CT19GENIChomozygous74716359
25321138253211383GC8GENIChomozygous74716363
25321141553211416GT6GENIChomozygous74716365
25321154253211543TG7GENICpossibly homozygous74716369
25321156853211569AG6GENIChomozygous74716371
25321230753212308CT31GENIChomozygous74716373
25321381853213819GT31GENIChomozygous74716375
25321382553213826CT29GENIChomozygous74716377
25321393753213938AG13GENICpossibly homozygous74716379
25321453553214536TG16GENIChomozygous74716383
25321647053216471GA26GENIChomozygous74716385
25321747353217474AG40GENIChomozygous74716387
25321502053215021CT9GENICpossibly homozygous75611782