chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32528358925283590TC9GENIChomozygous136661418
32528395825283959AG10GENIChomozygous136661419
32528427425284275AC11GENIChomozygous136661420
32528429425284295AG10GENIChomozygous136661421
32528446125284462TC15GENIChomozygous136661422
32528449625284497AG17GENIChomozygous136661423
32528451325284514CG15GENIChomozygous136661424
32528468225284683T14GENICheterozygous140984845
32528480925284810CT13GENIChomozygous136661425
32528544225285443AG17GENIChomozygous136661426
32528549125285492GA13GENIChomozygous136661427
32528555125285552AT9GENIChomozygous136661428
32528565425285655AG13GENIChomozygous136661429
32528610225286103GC5GENIChomozygous136661430
32528613625286137TC8GENIChomozygous136661431
32528621825286219AT15GENIChomozygous136661432
32528622525286226CT13GENIChomozygous136661433
32528632825286329TA15GENIChomozygous136661434
32528634225286343CT15GENIChomozygous136661435
32528634325286344CG15GENIChomozygous136661436
32528634525286346TA13GENIChomozygous136661437
32528652825286529TG20GENIChomozygous136661438
32528677825286779AT13GENIChomozygous136661439
32528710325287104CA22GENICpossibly homozygous136661440
32528749425287495AG13GENIChomozygous136661441
32528765325287654AT16GENIChomozygous136661442
32528810425288105CT17GENIChomozygous136661443
32528877125288772TG20GENIChomozygous136661444
32528877425288775TA20GENIChomozygous136661445
32528895925288960CT6GENIChomozygous136661446
32528896325288964CG7GENIChomozygous136661447
32528933925289340TG18GENIChomozygous136661448
32528969425289695AT15GENIChomozygous136661449
32529001625290017GA11GENIChomozygous136661451
32528494725284948G13GENICpossibly homozygous136553334
32528610125286102G5GENIChomozygous136553335
32528625525286257TG14GENIChomozygous136553336
32528842925288430A18GENIChomozygous136553337
32528880925288811AG19GENIChomozygous136553338
32528909625289096CA14GENIChomozygous136553339
32528978825289789TA12GENIChomozygous136661450
32528610125286102GT5GENICheterozygous154072712