Dear Glaxy users and admin

I ran my sequence data on FASTQC tool,
output says it is
Encoding Sanger / Illumina 1.9

now i want to groom my file, but groomer does not have option for 1.9 in "Input FASTQ quality scores type"

any idea which option i should select to grroom my file,

later i want to run Bowtie or Tophat,

Thanks