chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124105914941059150CCTGCAGA15GENIChomozygous50205308
124105969641059697CA21GENIChomozygous50205314
124106015641060157AG19GENIChomozygous50205315
124106028841060289CG14GENIChomozygous50323711
124106076541060766GA19GENIChomozygous50205317
124106102041061021AG10GENIChomozygous50422983
124106110241061103GA18GENIChomozygous50452629
124106130141061302GA24GENIChomozygous50205319
124106185441061855T-17GENIChomozygous50205321
124106227041062271G-12GENIChomozygous50205322
124106232241062323TC14GENIChomozygous50205323
124106236041062361GA17GENIChomozygous50571855
124106236141062362AG17GENIChomozygous50571857
124106237241062373TC17GENIChomozygous50323713
124106294741062948CT16GENIChomozygous50452630
124106483341064834AG18GENIChomozygous50205328
124106530341065304TA19GENIChomozygous50323719
124106722641067227A-24GENIChomozygous50205333
124106744841067450GG--2GENIChomozygous50205336
124106746341067464CT5GENIChomozygous50323726
124106748941067490CG9GENIChomozygous50205341
124106749441067495CT9GENIChomozygous50205342
124106769741067701AAAG----11GENIChomozygous50323728
124106781241067813TC9GENIChomozygous50205343
124107628941076297ACACACAC--------4GENICheterozygous50571859
124107632041076321CG12GENIChomozygous50205345
124107634141076408TAAACCTAAAGACATTTTAAAACAATTTTTTAAAGCTTTCACAGGAGTCTCAATCCTTAATGTCAGT-------------------------------------------------------------------11GENIChomozygous50512522