chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116982737116982738CT8GENIChomozygous117953918
8116985010116985011CT16GENIChomozygous117953919
8116985361116985362TC14GENIChomozygous117953920
8116987235116987236AG19GENIChomozygous116670619
8116987493116987494TC16GENIChomozygous117953923
8116989002116989003CA31GENIChomozygous117953924
8116989067116989068CT30GENICpossibly homozygous117953925
8116989671116989672CT21GENIChomozygous117953926
8116992452116992453GA15GENIChomozygous118111056
8116992647116992648GA15GENIChomozygous117953927