chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4148769196148769197CT32GENIChomozygous982044337
4148769696148769697AG27GENIChomozygous982044338
4148769955148769956TC16GENIChomozygous982044339
4148771044148771045TC26GENIChomozygous982044340
4148772789148772790AG20GENIChomozygous982044341
4148773824148773825AG20GENIChomozygous982044342
4148774153148774154TA31GENIChomozygous982044343
4148774940148774941CT10GENIChomozygous982044344
4148775642148775643AG36GENIChomozygous982044345
4148776170148776171AG27GENIChomozygous982044346
4148776221148776222TA32GENIChomozygous982044347
4148777251148777252AC15GENIChomozygous982044348
4148777452148777453CG14GENICheterozygous982044349
4148777909148777910AG18GENIChomozygous982044350
4148778302148778303AG16GENIChomozygous982044351
4148778783148778784CT20GENIChomozygous982044352
4148778826148778827GT21GENIChomozygous982044353
4148779100148779101TC11GENICpossibly homozygous982044354
4148779854148779855AG20GENIChomozygous982044355
4148781805148781806GA20GENIChomozygous982044356
4148781888148781889CT22GENIChomozygous982044357
4148782567148782568GT18GENIChomozygous982044358
4148783304148783305GA19GENIChomozygous982044359
4148783610148783611GC11GENIChomozygous982044360
4148784179148784180GA22GENIChomozygous982044361
4148785110148785111GA22GENIChomozygous982044362
4148785450148785451AG7GENIChomozygous982044363
4148785920148785921GC23GENIChomozygous982044364
4148786523148786524CG18GENIChomozygous982044365
4148787604148787605CT24GENIChomozygous982044366
4148791787148791788CA15GENIChomozygous982044367
4148791819148791820GA20GENIChomozygous982044368
4148793398148793399CT35GENIChomozygous982044369
4148793495148793496GA26GENIChomozygous982044370
4148793630148793631AT41GENIChomozygous982044371
4148796736148796737CA15GENIChomozygous982044372
4148797456148797457AC21GENIChomozygous982044373