chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13110741872110741873TC20GENIChomozygous967814630
13110742696110742697AG26GENIChomozygous967814631
13110743778110743779CT24GENIChomozygous967814632
13110743788110743789CT26GENIChomozygous967814633
13110743858110743859GA24GENIChomozygous967814634
13110743981110743982TC27GENIChomozygous967814635
13110744513110744514AG18GENIChomozygous967814636
13110744526110744527CT19GENIChomozygous967814637
13110744864110744865CT43GENIChomozygous967814638
13110745556110745557AG10GENIChomozygous967814639
13110745588110745589AG10GENIChomozygous967814640
13110745907110745908TA11GENIChomozygous967814641
13110746430110746431CT39GENIChomozygous967814642
13110746508110746509CT31GENIChomozygous967814643
13110746797110746798CT22GENIChomozygous967814644
13110747171110747172TC13GENIChomozygous967814645
13110748032110748033AC17GENIChomozygous967814646
13110748585110748586CT20GENIChomozygous967814647
13110748713110748714TC27GENIChomozygous967814648
13110748723110748724TC25GENIChomozygous967814649
13110748906110748907AG27GENIChomozygous967814650