Dear Mary,
You have basically 3 possibilities:
- Output the regions in a maf file (simple 'Output' filter)
- Output the regions in a single sequence file ('OutputAlignments' filter, with single file name. Several formats supported, including Fasta, Phylip, Clustal...)
- Output each region in a distinct file ('OutputAlignments' filter with special file name, for instance 'block-%i-%c-%b-%e.fasta' will create one fasta file for each block, including the block number, chromosome name, starting and ending positions in reference sequence. %c,%b and %e are optional, but %i is mandatory to create unique file names)
Hope this helps.
Best,
Julien.