chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190585791190585792GA26GENIChomozygous109178267
1190587208190587209AG3GENIChomozygous120510814
1190587210190587211AG3GENIChomozygous120510815
1190587212190587213AG4GENICheterozygous120811694
1190587214190587215AG4GENICheterozygous120848725
1190587216190587217AG3GENICheterozygous120848726
1190587876190587877GA24GENIChomozygous108465706
1190588459190588460GC17GENIChomozygous108465707
1190589874190589875AG14GENIChomozygous108465709
1190591839190591840GA18GENIChomozygous108465710
1190596155190596156AT18GENIChomozygous108465712
1190597825190597826TG22GENIChomozygous108465714
1190598462190598463TA17GENIChomozygous109178269
1190598463190598464CT16GENIChomozygous120781658
1190599318190599319CA12GENIChomozygous108465717
1190601531190601532CT23GENIChomozygous108465718
1190601782190601783AC26GENIChomozygous108465719
1190602553190602554CT27GENIChomozygous108465720
1190602709190602710GC26GENIChomozygous108465721
1190603902190603903GA13GENIChomozygous108465722
1190604689190604690CG20GENIChomozygous108465723