chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185058736185058737AT13GENIChomozygous659738785
4185058836185058837CCA3GENICheterozygous762865864
4185059168185059169AC7GENIChomozygous659738786
4185059565185059566CT41GENIChomozygous659738787
4185060079185060080TC16GENIChomozygous659738788
4185061023185061024AG20GENIChomozygous659738789
4185061177185061201CACACACACACACACACACACACG------------------------48GENICpossibly homozygous762865865
4185061541185061548GCGCAAG-------12GENIChomozygous762865866
4185061608185061609GA5GENIChomozygous659738790
4185061624185061625AAAAAAAAAC8GENIChomozygous762865867
4185061821185061822GA25GENIChomozygous659738791
4185062022185062023T-14GENIChomozygous762865868
4185062231185062232CT32GENIChomozygous659738792
4185062253185062254CA32GENIChomozygous659738793