chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25318958953189590CT11GENIChomozygous74716313
25319130153191302CA11GENIChomozygous78677212
25319175253191753CT23GENIChomozygous74716315
25319212853192129GT23GENIChomozygous74716317
25319253253192533TC29GENIChomozygous74716319
25319379853193799AT15GENIChomozygous74716321
25319426253194263AG24GENIChomozygous74716323
25319476653194767CT32GENIChomozygous74716325
25319511153195112GA23GENIChomozygous74716327
25319528153195282CT27GENIChomozygous74716329
25319575653195757CT20GENIChomozygous74716331
25319579653195797TA17GENIChomozygous74716333
25319612153196122GA21GENIChomozygous74716335
25319679853196799AG19GENIChomozygous74716337
25319698053196981CG27GENIChomozygous74716339
25319699753196998GA24GENIChomozygous74716341
25319733853197339AG12GENIChomozygous74716343
25319736353197364AG13GENIChomozygous74716345
25319743253197433TA9GENIChomozygous74716347
25319998953199990GC9GENICheterozygous74716351
25321024553210246CT22GENIChomozygous74716353
25321026653210267TC18GENIChomozygous74716355
25321030053210301CA8GENIChomozygous74716357
25321087953210880CT18GENIChomozygous74716359
25321138253211383GC9GENIChomozygous74716363
25321141553211416GT9GENIChomozygous74716365
25321142153211422TC9GENICpossibly homozygous74716367
25321154253211543TG7GENIChomozygous74716369
25321230753212308CT27GENIChomozygous74716373
25321381853213819GT25GENIChomozygous74716375
25321382553213826CT22GENIChomozygous74716377
25321393753213938AG19GENIChomozygous74716379
25321453553214536TG17GENIChomozygous74716383
25320024453200245GA18GENICheterozygous73604002
25321000153210002CA8GENICheterozygous73604006
25321502053215021CT14GENIChomozygous75611782
25321647053216471GA31GENIChomozygous74716385
25321747353217474AG33GENIChomozygous74716387