chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91714824417148245AG10GENICheterozygous51775659
91715913017159131TG58GENICheterozygous51775693
91716324917163250CG35GENICheterozygous51775709
91716845217168453CT39GENICheterozygous51775755
91716884617168847AG37GENICheterozygous51775757
91721469417214695GGT14GENICheterozygous51775893
91722851617228517AG33GENICheterozygous51775927
91724640417246405GC35GENICheterozygous51776003
91725931917259320GGT33GENICheterozygous51776028
91726859717268598AG28GENICheterozygous51776057
91729609517296096CT24GENICheterozygous51776125
91731342717313429AA--23GENICheterozygous51776223
91732987017329871C-22GENICheterozygous51776252
91735886717358868GA10GENICheterozygous51776366
91736316317363164GA12GENICheterozygous51776388
91736325517363256CG29GENICheterozygous51776390
91737695817376959TTACA30GENICheterozygous51776446
91737737417377375CT30GENICheterozygous51776448
91737774917377750CT23GENICheterozygous51776450
91738579017385791TC32GENICheterozygous51776488
91738581617385817TC28GENICheterozygous51776490
91739076417390765TG60GENICheterozygous51776507
91742419417424195AG33GENICheterozygous51776593
91742488917424890CA28GENICheterozygous51776597
91744657317446574GT34GENICheterozygous51776661
91745022017450221AG33GENICheterozygous51776683
91745038517450386CT19GENICheterozygous51776685
91745078417450785CA14GENICheterozygous51776687
91745462217454623TTA51GENICheterozygous51776695
91746026617460267AG31GENICheterozygous51776712
91747426217474263TC16GENICheterozygous51776740
91748229817482299CT14GENICheterozygous51776764