chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108897970888979709CA34INTERGENIChomozygous68157653
108897974288979743CG31INTERGENIChomozygous68157657
108898317688983177TG34GENIChomozygous68157660
108898348488983485CG2GENIChomozygous68157666
108898349788983498CA2GENIChomozygous68157669
108898396588983966CA32GENICheterozygous68157688
108898400188984002GC29GENIChomozygous68157691
108898415788984158AG38GENIChomozygous68157694
108898301088983011AG19GENIChomozygous68796746
108898364188983642TC31GENICheterozygous68796749
108898491188984912TA33GENIChomozygous68452796
108898513288985133AG23GENIChomozygous68452809
108898515888985159GC21GENIChomozygous68157715
108898533788985338GA45GENIChomozygous68796752
108898648688986487AG21INTERGENIChomozygous68157730
108898905688989057GA21INTERGENIChomozygous68796755
108899112288991123CT12INTERGENIChomozygous68796758
108899255488992555CG23INTERGENICheterozygous68796761
108899308088993081AG41INTERGENIChomozygous68157748
108899316088993161TC36INTERGENIChomozygous68157751
108899368188993682GA38INTERGENIChomozygous68796765
108899411788994118GA22INTERGENIChomozygous68796769
108899492988994930CT32INTERGENIChomozygous68796772
108899515788995158AG25INTERGENIChomozygous68157763
108899557688995577GT25INTERGENIChomozygous68157765
108899585788995858AG16INTERGENIChomozygous68796775
108899600388996004TC22INTERGENIChomozygous68157768
108899656888996569AG24INTERGENIChomozygous68157774
108899657588996576GA23INTERGENIChomozygous68157777
108899689588996896GT23INTERGENIChomozygous68796778