chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134760283747602838TC21GENIChomozygous947958331
134760429447604295TC25GENIChomozygous947958332
134760448347604484CT17GENIChomozygous947958333
134760449047604491CT14GENIChomozygous947958334
134760462947604630AC24GENIChomozygous947958335
134760488847604889TC22GENIChomozygous947958336
134760615447606155AT30GENIChomozygous947958337
134760690147606902CT26GENIChomozygous947958338
134760693447606935AG21GENIChomozygous947958339
134760701947607020AG32GENIChomozygous947958340
134760702747607028GA32GENIChomozygous947958341
134760728247607283GT20GENIChomozygous947958342
134760728947607290CT19GENIChomozygous947958343
134760745647607457AG18GENIChomozygous947958344
134760745747607458GA18GENIChomozygous947958345
134760753047607531GA20GENIChomozygous947958346
134760753447607535GT21GENIChomozygous947958347
134760757547607576GA25GENIChomozygous947958348
134760759147607592GC25GENIChomozygous947958349
134760761647607617GA30GENIChomozygous947958350
134760828147608282AG38GENIChomozygous947958351
134760874247608743AG14GENIChomozygous947958352
134760919247609193GA19GENIChomozygous947958353
134761003147610032TG16GENIChomozygous947958354
134761041847610419GA26GENIChomozygous947958355
134761069847610699CA35GENIChomozygous947958356
134761097447610975AG23GENIChomozygous947958357
134761107347611074AG19GENIChomozygous947958358
134761119947611200AT14GENIChomozygous947958359
134761143147611432AG23GENIChomozygous947958360
134761149747611498AG25GENIChomozygous947958361
134761298347612984CT16GENIChomozygous947958362
134761325247613253AG13GENIChomozygous947958363
134761349347613494AC15GENIChomozygous947958364
134761427947614280GA14GENIChomozygous947958365
134761443247614433AG10GENICpossibly homozygous947958366
134761464247614643GA16GENIChomozygous947958367
134761473647614737GA8GENIChomozygous947958368
134761473947614740GA8GENIChomozygous947958369
134761514747615148TC20GENIChomozygous947958370
134761631447616315AT27GENIChomozygous947958371