chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55949076359490764AG38GENIChomozygous113821649
55949103459491035GA36GENIChomozygous113821651
55949225259492253GA51GENIChomozygous113821653
55949242559492426AG27GENICpossibly homozygous113821655
55949329359493294TC35GENIChomozygous113821657
55949334459493345CT44GENIChomozygous113821659
55949402159494022GT40GENIChomozygous113821661
55949502159495022AG40GENIChomozygous113821663
55949624259496243AG49GENIChomozygous113821665
55949666359496664TA32GENICpossibly homozygous113821667
55949727059497271GA32GENIChomozygous113821669
55949929359499294GC36GENIChomozygous113821671
55950017959500180AG34GENIChomozygous113821673
55950082859500829GC52GENIChomozygous113821675
55950087359500874GA46GENIChomozygous113821677
55950087559500876CT48GENIChomozygous113821679
55950220759502208CA32GENIChomozygous113821681
55950224359502244CT35GENIChomozygous113821683
55950230059502301GA42GENIChomozygous113821685
55950234059502341CT47GENIChomozygous113821687
55950246859502469CT39GENIChomozygous113821689
55950268359502684TC40GENIChomozygous113821691
55950269859502699AT37GENIChomozygous113821693
55950274659502747AG26GENIChomozygous113821695
55950323259503233CT42GENIChomozygous113821701
55950324559503246CT36GENIChomozygous113821703
55950345359503454CT31GENIChomozygous113821705
55950351459503515TC38GENIChomozygous113821707
55950372059503721TC39GENIChomozygous113821709
55950411659504117TC28GENIChomozygous113821711
55950448859504489AG26GENIChomozygous113821713
55950488859504889TC38GENIChomozygous113821715
55950514059505141CT34GENIChomozygous113821717
55950546359505464TC55GENIChomozygous113821719
55950571859505719GA31GENIChomozygous113821721