chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108415374108415375CT17GENIChomozygous116908791
10108415789108415790GT16GENIChomozygous116908792
10108416505108416506AG17GENIChomozygous116908793
10108417104108417105AG20GENIChomozygous116908794
10108417302108417303GA18GENIChomozygous116908795
10108418140108418141CT14GENIChomozygous116908796
10108416220108416221TC22GENIChomozygous116715850
10108417681108417682TA17GENIChomozygous116715852
10108417831108417831T12GENICheterozygous132147732
10108418316108418316AGAG26GENIChomozygous132147733
10108418593108418594AC23GENIChomozygous116908798
10108418756108418757CT19GENIChomozygous116908799
10108418849108418850AG21GENIChomozygous116715858
10108418900108418901TC15GENIChomozygous116715861
10108419303108419304TC17GENIChomozygous116908800
10108419749108419750CT22GENIChomozygous116908801
10108419814108419815CT12GENIChomozygous116908802
10108419828108419829AT11GENIChomozygous116908803
10108419843108419844AT10GENIChomozygous116908804
10108420078108420078T12GENICheterozygous132331828
10108420294108420295GC18GENIChomozygous116715863
10108420753108420754AG27GENIChomozygous116908805
10108420882108420883GA20GENIChomozygous116908806
10108420991108420992AG16GENIChomozygous116908807
10108421070108421076GCGTTC19GENIChomozygous132147734
10108421143108421144TC18GENIChomozygous116908808
10108422041108422042AG18GENIChomozygous116715867
10108423293108423294AG22GENIChomozygous116908809
10108423371108423372AG23GENIChomozygous116908810
10108423745108423746AC24GENIChomozygous116715869
10108424629108424630AT23GENIChomozygous116908811
10108424868108424869AC12GENIChomozygous116908812
10108424940108424941TC10GENIChomozygous116961756
10108420138108420139CT20GENIChomozygous116961750
10108420145108420146AG20GENIChomozygous116961752
10108420147108420148CT20GENIChomozygous116961754