chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25318958953189590CT41GENIChomozygous74716313
25319175253191753CT27GENIChomozygous74716315
25319212853192129GT28GENIChomozygous74716317
25319253253192533TC43GENIChomozygous74716319
25319379853193799AT31GENIChomozygous74716321
25319426253194263AG50GENIChomozygous74716323
25319476653194767CT39GENIChomozygous74716325
25319511153195112GA35GENIChomozygous74716327
25319528153195282CT18GENIChomozygous74716329
25319575653195757CT36GENIChomozygous74716331
25319579653195797TA21GENIChomozygous74716333
25319612153196122GA49GENIChomozygous74716335
25319679853196799AG42GENIChomozygous74716337
25319698053196981CG41GENIChomozygous74716339
25319699753196998GA45GENIChomozygous74716341
25319733853197339AG29GENIChomozygous74716343
25319736353197364AG28GENIChomozygous74716345
25319743253197433TA28GENIChomozygous74716347
25319987353199874TG39GENICheterozygous74716349
25319998953199990GC22GENICheterozygous74716351
25321024553210246CT26GENIChomozygous74716353
25321026653210267TC21GENICpossibly homozygous74716355
25321030053210301CA9GENICheterozygous74716357
25321087953210880CT32GENICpossibly homozygous74716359
25321118353211184TC4GENICheterozygous74716361
25321141553211416GT6GENIChomozygous74716365
25321142153211422TC6GENIChomozygous74716367
25321154253211543TG10GENIChomozygous74716369
25321156853211569AG15GENIChomozygous74716371
25321230753212308CT42GENIChomozygous74716373
25321381853213819GT38GENIChomozygous74716375
25321382553213826CT36GENIChomozygous74716377
25321393753213938AG18GENICpossibly homozygous74716379
25321431253214313GA37GENICheterozygous74716381
25321453553214536TG47GENIChomozygous74716383
25321647053216471GA48GENIChomozygous74716385
25320902453209025GC17GENICheterozygous75806007
25321747353217474AG42GENIChomozygous74716387