chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119060337119060338AC21INTERGENIChomozygous115850883
7119062984119062985CT48INTERGENICpossibly homozygous118360057
7119064962119064963TG12INTERGENIChomozygous115850893
7119065312119065313CT22INTERGENIChomozygous115850895
7119065698119065699AC6INTERGENIChomozygous118332229
7119066088119066089CT17INTERGENIChomozygous116342471
7119066649119066650AG32INTERGENIChomozygous116342473
7119066839119066840AG45INTERGENIChomozygous116342475
7119067942119067943TG24INTERGENIChomozygous115850899
7119069568119069569CT20INTERGENIChomozygous116342479