chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181614119016141202ACATTCATGCTA37GENIChomozygous129518845
181614237716142378AG44GENIChomozygous110284367
181614212316142124CT44GENIChomozygous110284365
181614288516142886CT44GENIChomozygous110284369
181614875616148757CT43GENIChomozygous110284383
181614327316143280AGGACAA30GENIChomozygous131540212
181614328316143283TT31GENIChomozygous131540213
181614598916145989A17GENIChomozygous131540214
181615456116154562AT38GENIChomozygous110284403
181615501916155020TC46GENIChomozygous110284405
181615623116156232GT51GENIChomozygous110284407
181615935016159351T40GENIChomozygous129518852
181616330716163308TC48GENIChomozygous110284433
181617221916172220TC56GENICpossibly homozygous110284448
181617431216174313TC46GENIChomozygous110644396
181615350216153503GA36GENIChomozygous110644388
181615926216159263CT49GENIChomozygous110644389
181616394216163943CT56GENIChomozygous110644390
181616397616163977CT59GENIChomozygous110644391
181616639316166394AG48GENIChomozygous110644392
181616963516169636GA50GENIChomozygous110644393
181616963616169637CA50GENIChomozygous110644394
181617231816172319GA52GENIChomozygous110644395
181616449316164494TA43GENICpossibly homozygous110852992
181617552916175530GA48GENIChomozygous110284464
181617603416176035GA41GENIChomozygous110644397
181617813016178131GA51GENIChomozygous110644398
181617973116179732GA47GENIChomozygous110644399
181618148316181484GC48GENIChomozygous110644400
181618420916184210GA43GENIChomozygous110644401