chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103632801336328014GA20GENIChomozygous116560355
103632834136328342AG26GENIChomozygous116560357
103632848036328481TC24GENIChomozygous116560359
103632858736328588CA30GENIChomozygous116560361
103632969536329696TC33GENIChomozygous116560363
103632995736329958GA32GENIChomozygous116560365
103633003036330031TA24GENIChomozygous116560367
103633027736330278AC30GENIChomozygous116560369
103633053136330532GA35GENIChomozygous116560371
103633061336330614AC34GENIChomozygous116560373
103633063836330639TA27GENIChomozygous116560375
103633082036330821AG31GENIChomozygous116560377
103633135136331352CT35GENIChomozygous116560379
103633141536331416CG26GENIChomozygous116560381
103633150236331503AC32GENIChomozygous116560383
103633245536332456GA22GENIChomozygous116560385
103633281736332818GA35GENIChomozygous116560387
103633285236332853TC29GENIChomozygous116560389
103633286036332861CT30GENIChomozygous116560391
103633287036332871GT31GENIChomozygous116560393
103633304136333042AG31GENIChomozygous116560395
103633311136333112GA37GENIChomozygous116560397
103633341236333413CT29GENIChomozygous116560399
103633389836333899CT40GENIChomozygous116560401
103633498836334989GA36GENIChomozygous116560413
103633519836335199GA25GENIChomozygous116560415
103633526136335262AG29GENIChomozygous116560417
103633533136335332GA31GENIChomozygous116560419
103633536736335368GA26GENIChomozygous116560421
103633546136335462CT28GENIChomozygous116560423
103633547336335474CT31GENIChomozygous116560425
103633579636335797AG20GENIChomozygous116560427
103633586336335864GT21GENIChomozygous116560429
103633587736335878CT23GENIChomozygous116560431
103633592636335927GT32GENIChomozygous116560433
103633593836335939AG36GENIChomozygous116560435
103633598236335983CT34GENIChomozygous116560437
103633610836336109TA34GENIChomozygous116560439
103633611336336114TC33GENIChomozygous116560441
103633625336336254TC21GENIChomozygous116560443
103633641336336414GA19GENIChomozygous116560445
103633651536336516GC8GENIChomozygous116560447