chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153387685233876853AG19GENIChomozygous936348305
153387709333877094AG12GENIChomozygous936348306
153387722733877228CA19GENIChomozygous936348307
153387775433877755CT12GENIChomozygous936348308
153387777233877773AC11GENIChomozygous936348309
153387783733877838CG13GENIChomozygous936348310
153387785133877852CT14GENIChomozygous936348311
153387794133877942AC28GENIChomozygous936348312
153387827333878274TC23GENIChomozygous936348313
153387911733879118AT32GENIChomozygous936348314
153387959233879593CG22GENIChomozygous936348315
153388063033880631AG10GENIChomozygous936348316
153388188433881885CT16GENIChomozygous936348317
153388222133882222AG28GENIChomozygous936348318
153388295933882960TC27GENIChomozygous936348319
153388520733885208GA21GENIChomozygous936348320
153388702733887028CT25GENIChomozygous936348321
153388713833887139TC25GENIChomozygous936348322
153388723033887231CT22GENIChomozygous936348323
153388745533887456CG21GENIChomozygous936348324
153388770033887701CT14GENIChomozygous936348325
153388770133887702CT14GENIChomozygous936348326
153388841733888418TC18GENIChomozygous936348327
153388984333889844GA30GENICpossibly homozygous936348328