chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121607612160762CT23GENIChomozygous135482914
121628062162807CT26GENIChomozygous135482916
121628832162884TC24GENIChomozygous135482917
121660082166009AG27GENIChomozygous135482918
121661472166148TC18GENIChomozygous135482919
121669662166967AC20GENIChomozygous135482920
121681622168163AT15GENICheterozygous153786493
121683142168315CT27GENIChomozygous135482921
121697832169784AT36GENIChomozygous153786494
121735972173598CG21GENIChomozygous135482922
121750702175071TC14GENIChomozygous135482923
121757022175703AC33GENIChomozygous135482924
121860312186032TC27GENIChomozygous135482925
121681622168163A15GENICheterozygous402938833
121745492174551GG14GENICpossibly homozygous147887634
121745522174554TG14GENICpossibly homozygous147887635
121697832169784A36GENICheterozygous402938834
121711182171118A23GENICpossibly homozygous135390245
121727112172711T28GENIChomozygous135390246