chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144367053243670533TTA5GENICheterozygous740235707
144367059943670600A-9GENIChomozygous740235708
144367192543671926AG7GENICpossibly homozygous623422209
144367218343672184TTATAAA1GENIChomozygous740235709
144367233743672338TC32GENIChomozygous623422210
144367277143672772GA29GENICpossibly homozygous623422211
144367295643672957AG13GENICheterozygous623422212
144367343743673438AT17GENIChomozygous623422213
144367381643673817CT15GENICpossibly homozygous623422214
144367436243674363GA13GENIChomozygous623422215
144367437543674376TC14GENIChomozygous623422216
144367454943674550CG22GENIChomozygous623422217
144367495043674951GT16GENICheterozygous623422218
144367506243675063AAC3GENICheterozygous740235710
144367506243675063AACC3GENICheterozygous740235711
144367506243675063AACCC3GENICheterozygous740235712
144367511343675116AAA---5GENIChomozygous740235713
144367511943675120AG4GENIChomozygous623422219
144367525343675254CT12GENIChomozygous623422220
144367566243675663AG13GENICheterozygous623422221
144367662343676624AG10GENIChomozygous623422222