chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71150144411501445GA31GENIChomozygous952644362
71150162411501625GA36GENIChomozygous952644363
71150311911503120TC14GENIChomozygous952644364
71150324411503245GA17GENIChomozygous952644365
71150336111503362TC19GENIChomozygous952644366
71150349111503492GA15GENIChomozygous952644367
71150367411503675GC31GENIChomozygous952644368
71150392711503928AC27GENIChomozygous952644369
71150393411503935CT22GENIChomozygous952644370
71150394111503942TC23GENIChomozygous952644371
71150419411504195CT20GENIChomozygous952644372
71150510211505103AG29GENIChomozygous952644373
71150534411505345AC26GENIChomozygous952644374
71150538811505389CT19GENIChomozygous952644375
71150540111505402CT22GENIChomozygous952644376
71150550111505502CT16GENIChomozygous952644377
71150559611505597CT27GENIChomozygous952644378
71150645011506451GA24GENIChomozygous952644379
71150672911506730TC27GENIChomozygous952644380
71150682711506828AG17GENIChomozygous952644381
71150741711507418GA17GENIChomozygous952644382
71150743211507433TC19GENIChomozygous952644383
71150751411507515AG24GENIChomozygous952644384
71150753511507536AT19GENIChomozygous952644385
71150781711507818TC20GENIChomozygous952644386
71150783711507838GA25GENIChomozygous952644387
71150786811507869CT31GENIChomozygous952644388
71150854311508544TG17GENIChomozygous952644389
71150891111508912CT27GENIChomozygous952644390
71150969911509700AC18GENIChomozygous952644391
71150992511509926AG32GENIChomozygous952644392
71151030511510306CT18GENIChomozygous952644393
71151113711511138TC13GENIChomozygous952644394
71151125511511256CT27GENIChomozygous952644395
71151148011511481GA29GENIChomozygous952644396
71151176211511763GA34GENIChomozygous952644397
71151204611512047TC36GENIChomozygous952644398
71151214411512145GA28GENIChomozygous952644399
71151215911512160TC30GENIChomozygous952644400
71151247511512476TC13GENIChomozygous952644401
71151290311512904AC13GENIChomozygous952644402