chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153387685233876853AG22INTERGENIChomozygous787044296
153387691233876913GA20INTERGENIChomozygous787044297
153387709333877094AG26GENIChomozygous787044298
153387717033877171CT24GENIChomozygous787044299
153387722733877228CA22GENIChomozygous787044300
153387775433877755CT18GENIChomozygous787044301
153387785133877852CT23GENICpossibly homozygous787044302
153387794133877942AC21GENIChomozygous787044303
153387827333878274TC25GENIChomozygous787044304
153387911733879118AT19GENIChomozygous787044305
153387930933879310CT21GENIChomozygous787044306
153387935633879357TC24GENIChomozygous787044307
153387984433879845TC24GENIChomozygous787044308
153388063033880631AG15GENIChomozygous787044309
153388133833881339TC15GENIChomozygous787044310
153388222133882222AG18GENIChomozygous787044311
153388366533883666GA30GENIChomozygous787044312
153388520733885208GA29GENIChomozygous787044313
153388565133885652GA22GENIChomozygous787044314
153388668333886684CA18GENIChomozygous787044315
153388702733887028CT23GENIChomozygous787044316
153388713833887139TC27GENIChomozygous787044317
153388723033887231CT26GENIChomozygous787044318
153388770033887701CT20GENIChomozygous787044319
153388770133887702CT19GENIChomozygous787044320
153388811233888113GA28GENIChomozygous787044321
153388824133888242CT24GENICpossibly homozygous787044322
153388841733888418TC17GENIChomozygous787044323
153389060233890603GA15GENIChomozygous787044324
153389142633891427CT19GENIChomozygous787044325