chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182463585024635851GA12GENIChomozygous46393295
182463610724636108GA4GENIChomozygous46393296
182463756724637568TA10GENICpossibly homozygous46393297
182463793724637938CCGTGTGTAT3GENIChomozygous46393299
182463802324638024TG22GENICheterozygous46393300
182463841924638420AG23GENIChomozygous46393301
182463887324638874TG8GENICheterozygous46393303
182463981224639813CT23GENICheterozygous46393304
182464021824640219AG19GENIChomozygous46393305
182464052524640526AG27GENIChomozygous46393306
182464070724640708TG22GENICpossibly homozygous46393307
182464088324640884CT21GENIChomozygous46393308
182464093724640938CT13GENICheterozygous46393309
182464096824640969TC23GENICpossibly homozygous46393310
182464101524641016GA14GENIChomozygous46393311
182464125024641251CT22GENIChomozygous46393312
182464139124641392GGC1GENIChomozygous46393313
182464156924641570AG17GENICpossibly homozygous46393315
182464220824642209GA3GENIChomozygous46393317
182464222924642230GA11GENIChomozygous46393318
182464228524642286A-3GENIChomozygous46393319
182464230024642301AG7GENIChomozygous46393320
182464266724642668TC18GENIChomozygous46393321
182464287724642879CA--7GENICheterozygous46393322
182464293224642933AG12GENIChomozygous46393323