More documentation on output files

Hey guys, thx for the great tool!

I was just wondering whether I have missed something or is there just not more documentation on the output files available?

My specific questions:
1. **event_annotation.tsv**: What exactly are the columns (e.g. what do the columns genomic_start, and genomic_end display; why are not only splice-variants, but also the templates listed in this file?)
2. **sim_tx_info.txt**: What is the difference between foldchange.V1, and foldchange.c2? (What is V1, and what is c2?)