chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79962624799626248AG21GENIChomozygous116217672
79962716899627169TC16GENIChomozygous116260623
79963222599632226CT36GENIChomozygous116260625
79963494799634948TC45GENIChomozygous116217679
79963551999635520AG30GENIChomozygous116260626
79963911199639112TC12GENIChomozygous115785892
79963932799639328AG31GENIChomozygous116217684
79963961899639619GA23GENIChomozygous116260627
79964076699640767GA20GENIChomozygous116217690
79964145499641455TC12GENIChomozygous116260631
79964326999643270GT23GENIChomozygous116260632
79964387999643880CT31GENIChomozygous116260633
79964477799644778TC16GENIChomozygous116260634
79964578699645787AG29GENIChomozygous116260637
79964581299645813AT25GENIChomozygous116217692
79964755899647559GC26GENIChomozygous116260638
79964893599648936CT28GENIChomozygous116260639
79965106899651069GA29GENIChomozygous116260640
79965127399651274TA20GENIChomozygous116260641
79965178799651788CT34GENIChomozygous116260642
79965254399652544AG34GENIChomozygous116260643
79965331599653316AG31GENIChomozygous116217693
79965448599654486CT31GENIChomozygous115785900
79965476199654762AC25GENIChomozygous116260645
79965500599655006TC16GENIChomozygous116260646
79965535499655355TA34GENIChomozygous116260647
79965540499655405GA32GENIChomozygous116260648
79965615599656156TC35GENIChomozygous116260649
79965627399656274GA23GENIChomozygous116260650
79965824399658244AG25GENIChomozygous116260652
79966146299661463GT26GENIChomozygous116260653
79966171099661711GA20GENIChomozygous116260654
79966234999662350GA27GENIChomozygous116260655
79966273099662731GA20GENIChomozygous116260656
79966315799663158AG23GENIChomozygous116260657
79966377299663773AG22GENIChomozygous116217702
79966380799663808CT25GENIChomozygous116260658
79966958499669585CT14GENIChomozygous116260659
79967021699670217AC23GENIChomozygous116217705
79967147199671472TC32GENIChomozygous116217706
79967648799676488TC24GENIChomozygous116217713
79966893499668935CA21GENIChomozygous118339027