chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113118725731187258CT20GENIChomozygous115810702
113118944231189443GT10GENIChomozygous115810704
113118949031189491TC16GENIChomozygous115810706
113118993531189936TC17GENIChomozygous115810708
113119003831190039GA21GENIChomozygous115810710
113119149831191499AG33GENIChomozygous115810712
113119162931191630TC24GENIChomozygous115810714
113119166231191663CT16GENIChomozygous115810716
113119257831192579GA12GENIChomozygous115810718
113119349131193492AT10GENIChomozygous115810720
113119369631193697TG14GENIChomozygous115810722
113119514331195144AG10GENIChomozygous115810724
113119705331197054CT22GENIChomozygous115810726
113119769531197696CT4GENIChomozygous115810728
113119773331197734GA11GENIChomozygous115810732
113119791231197913CA9GENIChomozygous115810734
113120044131200442AG11GENIChomozygous115810738
113120105431201055CT23GENIChomozygous115810742
113120289831202899GA18GENIChomozygous115810744
113120302031203021GA6GENIChomozygous115810746
113120510231205103GA16GENIChomozygous115810748
113120804431208045CT4GENIChomozygous115810750
113120840131208402AG7GENICheterozygous115810752
113121012431210125CG13GENIChomozygous115810754
113121027231210273CA15GENIChomozygous115810756
113121223031212231AT10GENIChomozygous115810758
113121310931213110CT21GENIChomozygous115810762