chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25318958953189590CT17GENIChomozygous74716313
25319175253191753CT15GENIChomozygous74716315
25319212853192129GT23GENICpossibly homozygous74716317
25319253253192533TC18GENIChomozygous74716319
25319130153191302CA4GENICheterozygous78677212
25319379853193799AT20GENIChomozygous74716321
25319426253194263AG21GENIChomozygous74716323
25319476653194767CT13GENIChomozygous74716325
25319511153195112GA21GENIChomozygous74716327
25319528153195282CT17GENIChomozygous74716329
25319575653195757CT14GENICpossibly homozygous74716331
25319579653195797TA18GENIChomozygous74716333
25319612153196122GA22GENIChomozygous74716335
25319679853196799AG13GENIChomozygous74716337
25319698053196981CG22GENIChomozygous74716339
25319699753196998GA24GENIChomozygous74716341
25319733853197339AG17GENIChomozygous74716343
25319736353197364AG13GENIChomozygous74716345
25319743253197433TA9GENIChomozygous74716347
25319998953199990GC13GENIChomozygous74716351
25321024553210246CT12GENIChomozygous74716353
25321026653210267TC8GENIChomozygous74716355
25321030053210301CA9GENICheterozygous74716357
25321087953210880CT23GENICpossibly homozygous74716359
25321138253211383GC3GENIChomozygous74716363
25321141553211416GT6GENIChomozygous74716365
25321142153211422TC8GENIChomozygous74716367
25321154253211543TG6GENIChomozygous74716369
25321156853211569AG10GENIChomozygous74716371
25321230753212308CT20GENIChomozygous74716373
25321381853213819GT20GENICpossibly homozygous74716375
25321382553213826CT19GENICpossibly homozygous74716377
25321393753213938AG10GENICpossibly homozygous74716379
25321453553214536TG17GENIChomozygous74716383
25321647053216471GA15GENICpossibly homozygous74716385
25321747353217474AG35GENIChomozygous74716387
25320024453200245GA13GENICheterozygous73604002
25321000153210002CA6GENICheterozygous73604006
25321502053215021CT7GENIChomozygous75611782