Dear Galaxy staff,

I have recently started using your tool and it has been really helpful,
thank you!
When using Human Genome Variation, aaChanges, I would like to keep some
extra lines in the output file from either of the input files. In the tool
description it says I should be able to keep them:

"...chromosome, start, and end position as well as the SNP. The SNP can be
given using ambiguous-nucleotide symbols or a list of two to four alleles
separated by '/'. *Any other columns in the first input file will not be
used but will be kept for the output*. The second input file contains..."

However, I haven't found a way of actually have them in the output file.
What am I missing/doing incorrectly?
What I've been trying to keep by the way is rs IDs or Ensembl gene IDs.

Thank you in advance for your answer.
Kind regards,

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