chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122556860625568607AG24GENIChomozygous50141415
122556864925568650CT23GENIChomozygous50141418
122556937225569373CT34GENIChomozygous50141420
122556957925569580TC34GENIChomozygous50141422
122556977725569778CT25GENICpossibly homozygous50141424
122557031125570312GGGGGA1GENIChomozygous50611429
122557073525570736CT32GENIChomozygous50141428
122557139125571392AG29GENIChomozygous50141430
122557184925571853AGTG----30GENIChomozygous50141432
122557200725572008GA35GENIChomozygous50141434
122557226925572270AAT19GENIChomozygous50141436
122557231925572320TC21GENIChomozygous50141438
122557255125572552GA11GENIChomozygous50141440
122557258725572600TAGCAAACACGAG-------------9GENIChomozygous50141442
122557261525572616TTC6GENIChomozygous50141444
122557263725572638GGAAACA12GENIChomozygous50141446
122557276325572764AG15GENIChomozygous50141448
122557287725572878AG37GENIChomozygous50141450
122557355125573552TC19GENIChomozygous50141452
122557357625573577GC16GENIChomozygous50141454
122557382625573827AT22GENIChomozygous50141460
122557361225573613AG22GENIChomozygous50141456
122557371925573720TC16GENIChomozygous50141458
122557418325574184GA30GENIChomozygous50141462
122557437625574377AC25GENIChomozygous50141464
122557437925574380CT30GENIChomozygous50141466
122557445325574454AC31GENIChomozygous50141468