chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130102929130102934TTTCT-----2INTERGENIChomozygous54110320
7130102937130102938TG2INTERGENIChomozygous55010344
7130103860130103861CCAA11INTERGENIChomozygous54110321
7130104127130104128AG11INTERGENIChomozygous54110322
7130105399130105400CG24INTERGENIChomozygous54110323
7130105876130105877TC19INTERGENICheterozygous54110324
7130105906130105907GA18INTERGENICpossibly homozygous54110325
7130107591130107592GA22INTERGENIChomozygous54110326
7130107830130107831AC11INTERGENIChomozygous54110327
7130108303130108304CT15INTERGENIChomozygous54110328