chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25318958953189590CT43GENIChomozygous74716313
25319130153191302CA3GENIChomozygous78677212
25319175253191753CT52GENIChomozygous74716315
25319212853192129GT20GENIChomozygous74716317
25319253253192533TC21GENICpossibly homozygous74716319
25319379853193799AT30GENIChomozygous74716321
25319426253194263AG23GENIChomozygous74716323
25319476653194767CT32GENIChomozygous74716325
25319511153195112GA31GENIChomozygous74716327
25319528153195282CT31GENIChomozygous74716329
25319575653195757CT41GENIChomozygous74716331
25319579653195797TA33GENIChomozygous74716333
25319612153196122GA14GENIChomozygous74716335
25319679853196799AG26GENIChomozygous74716337
25319698053196981CG21GENIChomozygous74716339
25319699753196998GA24GENIChomozygous74716341
25319733853197339AG30GENIChomozygous74716343
25319736353197364AG27GENIChomozygous74716345
25319743253197433TA18GENIChomozygous74716347
25319998953199990GC14GENICheterozygous74716351
25321024553210246CT29GENIChomozygous74716353
25321026653210267TC20GENICpossibly homozygous74716355
25321030053210301CA11GENICpossibly homozygous74716357
25321087953210880CT44GENICpossibly homozygous74716359
25321118353211184TC7GENIChomozygous74716361
25321138253211383GC10GENIChomozygous74716363
25321141553211416GT4GENIChomozygous74716365
25321142153211422TC5GENIChomozygous74716367
25321154253211543TG10GENIChomozygous74716369
25321156853211569AG15GENIChomozygous74716371
25321230753212308CT41GENICpossibly homozygous74716373
25321381853213819GT22GENIChomozygous74716375
25321382553213826CT24GENIChomozygous74716377
25321393753213938AG32GENIChomozygous74716379
25321453553214536TG24GENIChomozygous74716383
25321647053216471GA19GENIChomozygous74716385
25321747353217474AG27GENIChomozygous74716387
25320024453200245GA26GENICheterozygous73604002
25321000153210002CA4GENICheterozygous73604006
25321502053215021CT16GENIChomozygous75611782