chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159922785499227855TG4GENIChomozygous112614297
159922785799227858TG4GENIChomozygous112995156
159922786099227861TG4GENIChomozygous113072415
159922801499228015AG8GENIChomozygous112614301
159922813199228132TC15GENIChomozygous112614303
159922813299228133AG15GENIChomozygous112614305
159922828099228281CT11GENIChomozygous112614307
159922834199228342TC7GENIChomozygous112614309
159922836199228362TG10GENIChomozygous112614311
159922884099228841CT14GENIChomozygous112614313
159922943599229436CA17GENICpossibly homozygous112614315
159922946999229470TG18GENIChomozygous112614317
159922981299229813AG16GENIChomozygous112614319
159922985999229860TC16GENIChomozygous112614321
159923010999230110TG9GENIChomozygous112614323
159923054599230546TC18GENIChomozygous112614327
159923059299230593TC23GENIChomozygous112826261
159923076899230769GA12GENIChomozygous112614329
159923079599230796TC15GENIChomozygous112614331
159923084699230847CT15GENIChomozygous112614333
159923111599231116CT16GENIChomozygous112614335
159923113999231140TC19GENIChomozygous112614337
159923114199231142GT20GENIChomozygous112614339
159923116999231170GT20GENIChomozygous112614341
159923118599231186TC18GENIChomozygous112614343
159923158199231582TC12GENIChomozygous112614345
159923180199231802AT18GENIChomozygous112614347
159923188599231886TG16GENIChomozygous112614349
159923234299232343AT25GENIChomozygous112614351
159923246599232466TA18GENIChomozygous112759723
159923256599232566AT14GENIChomozygous112614353
159923257999232580TC12GENIChomozygous112614355
159923261399232614TC13GENIChomozygous112826263
159923277299232773TG23GENIChomozygous112614357
159923282399232824GA23GENIChomozygous112614359
159923286599232866TC17GENIChomozygous112614361
159923288599232886AG20GENIChomozygous112614363
159923293799232938GA22GENIChomozygous112614365
159923297199232972GA29GENIChomozygous112826265
159923315999233160CG25GENIChomozygous112614367