chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91714824417148245AG17GENICheterozygous51775659
91715913017159131TG54GENICheterozygous51775693
91716324917163250CG47GENICheterozygous51775709
91716845217168453CT49GENICheterozygous51775755
91716884617168847AG62GENICheterozygous51775757
91721469417214695GGT26GENICheterozygous51775893
91722851617228517AG50GENICheterozygous51775927
91724640417246405GC37GENICheterozygous51776003
91725931917259320GGT37GENICheterozygous51776028
91726859717268598AG57GENICheterozygous51776057
91729609517296096CT21GENICheterozygous51776125
91731342717313429AA--24GENICheterozygous51776223
91732987017329871C-33GENICheterozygous51776252
91735886717358868GA18GENICheterozygous51776366
91736316317363164GA18GENICheterozygous51776388
91736325517363256CG45GENICheterozygous51776390
91737695817376959TTACA20GENICheterozygous51776446
91737737417377375CT25GENICheterozygous51776448
91737774917377750CT33GENICheterozygous51776450
91738579017385791TC54GENICheterozygous51776488
91738581617385817TC53GENICheterozygous51776490
91739076417390765TG62GENICheterozygous51776507
91742419417424195AG33GENICheterozygous51776593
91742488917424890CA22GENICheterozygous51776597
91744657317446574GT39GENICheterozygous51776661
91745022017450221AG29GENICheterozygous51776683
91745038517450386CT20GENICheterozygous51776685
91745078417450785CA6GENICheterozygous51776687
91745462217454623TTA43GENICheterozygous51776695
91746026617460267AG62GENICheterozygous51776712
91747426217474263TC16GENICheterozygous51776740
91748229817482299CT35GENICheterozygous51776764