chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166221270162212701A25GENIChomozygous129371925
166221501762215021GGGG7GENIChomozygous129371926
166223372262233723TG18GENICpossibly homozygous111839569
166223688562236888CCC12GENIChomozygous129371927
166223688862236889CG12GENIChomozygous112309852
166223689062236891CA12GENIChomozygous112131697
166223689262236893CT12GENIChomozygous112309854
166223733962237339T3GENIChomozygous129371928
166223696162236962CT9GENIChomozygous119121053
166223610362236104CA3GENICheterozygous112263455
166223689462236895CG12GENIChomozygous119121052