chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25318958953189590CT45GENIChomozygous74716313
25319175253191753CT25GENIChomozygous74716315
25319212853192129GT28GENIChomozygous74716317
25319253253192533TC50GENIChomozygous74716319
25319379853193799AT22GENIChomozygous74716321
25319426253194263AG29GENICpossibly homozygous74716323
25319476653194767CT29GENIChomozygous74716325
25319511153195112GA23GENIChomozygous74716327
25319528153195282CT38GENICpossibly homozygous74716329
25319575653195757CT27GENIChomozygous74716331
25319579653195797TA30GENIChomozygous74716333
25319612153196122GA35GENIChomozygous74716335
25319679853196799AG24GENIChomozygous74716337
25319698053196981CG37GENIChomozygous74716339
25319699753196998GA46GENIChomozygous74716341
25319733853197339AG29GENIChomozygous74716343
25319736353197364AG34GENIChomozygous74716345
25319743253197433TA23GENIChomozygous74716347
25319751253197513CT10GENICheterozygous75354174
25319966253199663TC34GENICheterozygous75354175
25319987353199874TG60GENICheterozygous74716349
25319998953199990GC19GENICheterozygous74716351
25321024553210246CT23GENICheterozygous74716353
25321026653210267TC11GENICheterozygous74716355
25321030053210301CA6GENICheterozygous74716357
25321087953210880CT47GENICpossibly homozygous74716359
25321118353211184TC12GENICheterozygous74716361
25321138253211383GC10GENICpossibly homozygous74716363
25321141553211416GT12GENICheterozygous74716365
25321142153211422TC18GENICheterozygous74716367
25321154253211543TG17GENICheterozygous74716369
25321156853211569AG17GENICheterozygous74716371
25321230753212308CT32GENIChomozygous74716373
25321381853213819GT42GENIChomozygous74716375
25321382553213826CT40GENIChomozygous74716377
25321393753213938AG23GENICheterozygous74716379
25321431253214313GA37GENICheterozygous74716381
25321433253214333GA61GENICheterozygous75354176
25321435353214354TC47GENICheterozygous75354177
25321453553214536TG31GENIChomozygous74716383
25321647053216471GA31GENIChomozygous74716385
25321747353217474AG34GENIChomozygous74716387