a3b7988cbb4a1fa6c2bba2d3120fdff0889de05d
jnavarr5
  Thu Jun 26 16:09:52 2025 -0700
Fixing a typo reported by Bob, refs #35974

diff --git src/hg/htdocs/inc/recTrackSets.hg19.tab src/hg/htdocs/inc/recTrackSets.hg19.tab
index 1fd218a3767..0794c4bf6f4 100644
--- src/hg/htdocs/inc/recTrackSets.hg19.tab
+++ src/hg/htdocs/inc/recTrackSets.hg19.tab
@@ -1,16 +1,16 @@
 # List of curated sessions for clinical, etc. users
 #
 # File is tab-separated.  userName and sessionName are fields in hgcentral.namedSessionDb table
 #       sessionName is cgi-decoded to readable text
 # Note that named sessions support description in settings field, however the description in
 #       this file is used in browser (allows non-owner of session, e.g. QA, to edit)
 #       
 # For details on how to update this file, see the wiki: http://genomewiki.ucsc.edu/genecats/index.php/Recommended_Track_Sets
 #       
 # Format: label, userName, sessionName, description
 Clinical SNVs	View	SNVs%20Clinical	Assess potential disease contributions of single nucleotide variants in coding regions
 Clinical CNVs	View	CNVs%20Clinical	Assess potential disease contributions of structural variants in coding regions
 Non-coding SNVs	View	Non%20coding%20SNVs	Investigate functional aspects of non-coding variants
 Determine Exon Relevance	View	Exon_Relevance_hg19	Examine if variants are present in an exon required for the function of the expressed gene product
 Problematic Regions	View	Problematic%20Regions	Evaluate if annotations are on potential low confidence regions due to high homology or other reported concerns
-ENIGMA BRCA1/BRCA2 VCEP	View	BRCA1_BRCA2_ENIGMA_hg19	Asses potential disease contribution of variants on BRCA1 and BRCA2 according to the ENIGMA VCEP guidelines
+ENIGMA BRCA1/BRCA2 VCEP	View	BRCA1_BRCA2_ENIGMA_hg19	Assess potential disease contribution of variants on BRCA1 and BRCA2 according to the ENIGMA VCEP guidelines