chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35596179555961796GA22GENIChomozygous112124330
35596186355961864AT32GENIChomozygous111577559
35596431355964314AG16GENIChomozygous112124331
35596744655967447GA21GENICheterozygous111909908
35596745455967455GA21GENICheterozygous111909909
35596745855967459GA19GENICpossibly homozygous112124332
35596746255967463GA20GENICheterozygous112124333
35596747055967471GA18GENICpossibly homozygous112124334
35597012055970121CT11GENIChomozygous112124335
35597052655970527TC27GENIChomozygous111577582
35597257455972575TG24GENIChomozygous112124336
35597542955975430AC17GENIChomozygous111577592
35597551555975516TG24GENICheterozygous112124337
35597703355977034CG27GENIChomozygous111577595
35597782755977828AT13GENIChomozygous112124338
35598104155981042CA21GENIChomozygous112124339
35598331555983316GA23GENIChomozygous112124340
35598405255984053CA35GENIChomozygous112124341
35598421555984216CA17GENIChomozygous112124342
35598441655984417TC19GENIChomozygous112124343
35598446255984463TG15GENICpossibly homozygous112124344
35598448055984481TC22GENICheterozygous112124345
35598558155985582CA24GENIChomozygous112124346
35598562255985623GA22GENIChomozygous112124347
35598570555985706CT32GENIChomozygous112124348
35598620555986206CT15GENIChomozygous111577604
35598627255986273AG22GENIChomozygous111577605
35598717355987174GA34GENICheterozygous111577617
35598718055987181AG34GENICheterozygous111577618
35598718755987188GC32GENICheterozygous111577619
35598720455987205CT25GENICheterozygous111577620
35598720755987208GA23GENICheterozygous111577621
35598721355987214AG24GENICheterozygous111577622
35598722955987230CG24GENICheterozygous111577623
35598725155987252AG24GENICheterozygous111577624
35598799155987992CT28GENIChomozygous111577626
35598818355988184TA28GENIChomozygous112124349
35598959655989597CT12GENIChomozygous112124350