chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185058736185058737AT16GENIChomozygous652143787
4185058836185058837CCA7GENICpossibly homozygous758325022
4185059168185059169AC20GENIChomozygous652143788
4185059565185059566CT18GENIChomozygous652143789
4185060079185060080TC19GENIChomozygous652143790
4185061023185061024AG20GENIChomozygous652143791
4185061177185061201CACACACACACACACACACACACG------------------------18GENICpossibly homozygous758325023
4185061541185061548GCGCAAG-------7GENIChomozygous758325024
4185061608185061609GA5GENIChomozygous652143792
4185061624185061625AAAAAAAAAC8GENIChomozygous758325025
4185061821185061822GA14GENIChomozygous652143793
4185062022185062023T-18GENIChomozygous758325026
4185062231185062232CT12GENIChomozygous652143794
4185062253185062254CA13GENIChomozygous652143795