chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122092445720924458C-20GENICheterozygous50107346
122092448720924488CT27GENICpossibly homozygous50107348
122092450820924509CCCT27GENIChomozygous50107350
122092482420924826GT--32GENICheterozygous50107352
122092483320924845TGTGTGTGTGTC------------37GENIChomozygous50107354
122092483520924836TTCTG42GENICheterozygous50107356
122092498720924988CT29GENIChomozygous50107358
122092499920925000GA32GENIChomozygous50107360
122092508920925090TC26GENIChomozygous50107362
122092541320925414AG26GENIChomozygous50107364
122092545420925455GA28GENIChomozygous50107366
122092627320926274TC19GENIChomozygous50107368
122092633020926331AAT21GENIChomozygous50107370
122092665620926657GGA17GENICpossibly homozygous50107372
122092695620926962TAGGTT------18GENIChomozygous50107374
122092736920927370C-29GENIChomozygous50107376
122092757220927582AGAAAGAAAG----------9GENIChomozygous50107378
122092760820927610AG--8GENICpossibly homozygous50107382
122092763120927632AAG9GENICheterozygous50107384
122092764020927641AG4GENIChomozygous50107388
122092764420927645AG6GENICheterozygous50107390
122092770920927710AG8GENICheterozygous50107392
122092773520927737AA--4GENICheterozygous50107398
122092775420927755G-7GENICheterozygous50107400
122092775420927755GGA7GENICheterozygous50107402
122092784420927845TC22GENIChomozygous50107404
122092803820928039CT6GENIChomozygous50107406
122092832520928326CCT4GENICheterozygous50107408
122092832520928326CCTT4GENICheterozygous50107410
122092886020928861AT18GENIChomozygous50107412
122092946220929463TC9GENIChomozygous50107414
122093009220930093CT25GENIChomozygous50107416
122093023520930236AAT8GENIChomozygous50107418
122093063220930633CCT18GENIChomozygous50107420
122093073520930736GA20GENIChomozygous50107422
122093129020931291GT47GENICheterozygous50107424
122093143220931433CG45GENICheterozygous50402178