Hi,

I have a genomic region of interest, and I want to extract all the exon 
coordinates for sequence capture. The annotation database I want to use is the 
UCSC Known Genes database. 

However, it seems to me that the Known Genes database contains splice variants 
for several genes. I just want the start and stop coordinates of all exons 
(both coding and non-coding, and both known and novel) within my region of 
interest, without any duplicated exons. Any idea on how this can be done?

Thanks,
Joses
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