chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2003776920037770GA10GENIChomozygous108544281
X2003841020038411AC13GENIChomozygous108544283
X2003879220038793AT19GENICpossibly homozygous108544285
X2003884820038849CT20GENIChomozygous108236278
X2004260420042605TC10GENICpossibly homozygous108700848
X2004497220044973GC17GENIChomozygous108236284
X2004510820045109GA18GENICpossibly homozygous108544287
X2004649620046497CT13GENICpossibly homozygous108544289
X2005295720052958CT12GENIChomozygous108544291
X2005305620053057CA12GENIChomozygous108544293
X2005306920053070TC12GENIChomozygous108236286
X2005381720053818TC17GENIChomozygous108544295
X2005409920054100CT11GENICheterozygous108236290
X2005667820056679AG11GENICheterozygous108236294
X2005988720059888AC15GENICpossibly homozygous108544297
X2006371720063718GA19GENIChomozygous108236304
X2006719820067199AG18GENIChomozygous108544299
X2006755320067554CA12GENIChomozygous108236315
X2006779120067792AG12GENIChomozygous108236317
X2006904920069050AG7GENIChomozygous108236319
X2004936920049370AT17GENICpossibly homozygous108789932
X2005895820058959TC11GENIChomozygous108476220
X2005896620058967TG11GENIChomozygous108476222