chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144702236144702237CT17GENIChomozygous114037634
5144703487144703488TC12GENIChomozygous114037635
5144705741144705742CG32GENIChomozygous114037636
5144707032144707033AC5GENIChomozygous114037637
5144707830144707831TC12GENIChomozygous114037638
5144711340144711341TG27GENIChomozygous114037639
5144712781144712782TA13GENIChomozygous114037640
5144718691144718692CG14GENIChomozygous114037641
5144719730144719731CT27GENIChomozygous114037642
5144721912144721913CT24GENIChomozygous114037643
5144722327144722328GT23GENIChomozygous114037644
5144722336144722337TG24GENIChomozygous114037645
5144722347144722348GA24GENIChomozygous114037646
5144722355144722356AG23GENIChomozygous114037647
5144722397144722398AT28GENICpossibly homozygous114037648
5144722422144722423CT20GENIChomozygous114037649
5144722424144722425GT20GENICpossibly homozygous114037650
5144722430144722431AT20GENIChomozygous114037651
5144722438144722439CT24GENIChomozygous114037652
5144722445144722446GA25GENIChomozygous114037653
5144722457144722458CT29GENIChomozygous114037654
5144722478144722479GT25GENIChomozygous114037655
5144722606144722607GT31GENIChomozygous114037659
5144723042144723043GT23GENIChomozygous114037660
5144723231144723232AG14GENICheterozygous114037661
5144723329144723330CT15GENICheterozygous114037662
5144724477144724478TG13GENIChomozygous114037663
5144726927144726928AG22GENIChomozygous114037664
5144729165144729166CG23GENIChomozygous114037665
5144729514144729515CT9GENIChomozygous114037666
5144730051144730052AG18GENIChomozygous114037667
5144731121144731122CA11GENIChomozygous114037668
5144731711144731712CT27GENIChomozygous114037669
5144733565144733566CT25GENIChomozygous114037670
5144733613144733614GA19GENIChomozygous114037671
5144733725144733726TC28GENIChomozygous114037672