chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103632834136328342AG19GENIChomozygous116560357
103632848036328481TC23GENIChomozygous116560359
103632858736328588CA22GENIChomozygous116560361
103632969536329696TC16GENIChomozygous116560363
103632995736329958GA18GENIChomozygous116560365
103633003036330031TA18GENIChomozygous116560367
103633027736330278AC25GENIChomozygous116560369
103633053136330532GA30GENIChomozygous116560371
103633061336330614AC28GENIChomozygous116560373
103633063836330639TA28GENIChomozygous116560375
103633082036330821AG34GENIChomozygous116560377
103633135136331352CT30GENIChomozygous116560379
103633141536331416CG30GENIChomozygous116560381
103633150236331503AC32GENIChomozygous116560383
103633245536332456GA21GENIChomozygous116560385
103633266136332662TC19GENIChomozygous116758925
103633281736332818GA21GENIChomozygous116560387
103633285236332853TC14GENIChomozygous116560389
103633286036332861CT17GENIChomozygous116560391
103633287036332871GT17GENIChomozygous116560393
103633304136333042AG19GENIChomozygous116560395
103633311136333112GA18GENIChomozygous116560397
103633341236333413CT31GENIChomozygous116560399
103633438436334385GT1GENIChomozygous116560405
103633498836334989GA20GENIChomozygous116560413
103633526136335262AG24GENIChomozygous116560417
103633533136335332GA26GENIChomozygous116560419
103633546136335462CT26GENIChomozygous116560423
103633547336335474CT26GENIChomozygous116560425
103633579636335797AG17GENIChomozygous116560427
103633586336335864GT23GENICpossibly homozygous116560429
103633587736335878CT21GENIChomozygous116560431
103633592636335927GT16GENIChomozygous116560433
103633593836335939AG19GENIChomozygous116560435
103633625336336254TC16GENIChomozygous116560443
103633641336336414GA17GENIChomozygous116560445
103633651536336516GC4GENIChomozygous116560447