chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121607612160762CT20GENIChomozygous135482914
121628062162807CT17GENIChomozygous135482916
121628832162884TC22GENIChomozygous135482917
121660082166009AG18GENIChomozygous135482918
121661472166148TC21GENIChomozygous135482919
121669662166967AC16GENIChomozygous135482920
121683142168315CT17GENIChomozygous135482921
121735972173598CG14GENIChomozygous135482922
121750702175071TC23GENIChomozygous135482923
121681622168163A5GENICheterozygous402938833
121681622168163AT5GENIChomozygous153786493
121697832169784AT20GENIChomozygous153786494
121739712173973GT3GENIChomozygous148244513
121745492174551GG8GENIChomozygous147887634
121745522174554TG8GENIChomozygous147887635
121757022175703AC25GENIChomozygous135482924
121860312186032TC23GENIChomozygous135482925
121697832169784A20GENICheterozygous402938834
121711182171118A17GENIChomozygous135390245
121727112172711T18GENIChomozygous135390246