chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8119074818119074818T19GENICpossibly homozygous138268900
8119075538119075539CT13GENIChomozygous138433765
8119075571119075572CA10GENIChomozygous138433766
8119075952119075952C8GENIChomozygous138268901
8119076340119076341TC20GENIChomozygous142104989
8119076832119076833CT5GENIChomozygous138433768
8119077146119077147TC10GENIChomozygous138433769
8119077162119077163AG9GENIChomozygous138433770
8119077429119077430GA9GENIChomozygous138433771
8119077450119077451TC8GENIChomozygous138433772