chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155681820155681821TTA12GENIChomozygous58089381
4155683619155683620GC23GENIChomozygous58089383
4155683941155683942CCGGG5GENIChomozygous58089385
4155685385155685386GT31GENICpossibly homozygous58089389
4155686017155686018AG16GENIChomozygous57526714
4155686660155686661AT35GENIChomozygous58089391
4155687107155687108TG22GENIChomozygous58089393
4155688536155688537GGTTTT11GENIChomozygous57526724
4155688566155688567GGTTA17GENIChomozygous58287271
4155688620155688621GA16GENIChomozygous58089395
4155688894155688899GGTTC-----14GENIChomozygous57526730
4155691020155691021AAT12INTERGENICheterozygous57526750
4155688537155688538GT11GENIChomozygous58348313
4155688958155688959GC14GENIChomozygous58089397
4155690734155690735CG12INTERGENIChomozygous58089399
4155690760155690761CT10INTERGENIChomozygous58089401
4155689322155689323AC17GENIChomozygous57526740
4155691021155691022T-12INTERGENICheterozygous58089403