chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98152465181524652T30GENICheterozygous129959679
98152487881524879G16GENIChomozygous128727711
98152488681524887AG14GENIChomozygous117380938
98152488981524890C15GENIChomozygous128727712
98152492381524924C9GENIChomozygous128727713
98152492481524925CG9GENIChomozygous123206641
98152493181524931C8GENIChomozygous128727714
98152494181524941CC7GENIChomozygous128727715
98152494581524945C6GENIChomozygous128727716
98152496381524963TCT7GENIChomozygous128727717
98152497281524973C8GENIChomozygous128727718
98152503281525033T13GENIChomozygous128727719
98152504781525048T16GENIChomozygous128727720
98152658281526583GT16GENIChomozygous117380939