-CMSets table
trans_id: reference transcript id (e.g. NM_032211.6)      
var_id: variant id (refer to dbSNP, e.g. rs141995277)  
score: single variant score in a set (scored by HMMvar).    
hgvs: HGVS name of the variant.    
setID: set id, indicating the set a variant belongs to.
setScore: the whole set score (scored by HMMvar).

-nonCMSets table
trans_id: reference transcript id (e.g. NM_032211.6)
var_id: variant id (refer to dbSNP, e.g. rs141995277)  
score: single variant score in a set (scored by HMMvar).    
hgvs: HGVS name of the variant.    
setID: set id, indicating the set a variant belongs to.
setScore: the whole set score (scored by HMMvar).

-Set scores table
individual_id: individual ids from the 1000 Genomes Project (e.g.HG00428) 
trans_id: reference transcript id (e.g. NM_032211.6)         
variant_name: variant id (refer to dbSNP, e.g. rs141995277)     
set_id: set id, indicating the set a variant belongs to.
score: the whole set score (scored by HMMvar).

-Single scores table
var_id: variant id (refer to dbSNP, e.g. rs141995277)    
trans_id: reference transcript id (e.g. NM_032211.6)        
pos: the position of a variant with respect to the corresponding transcript.      
mRNAref: the reference allele. 
mRNAalt: the alternative allele.
score: single variant score in a set (scored by HMMvar).    
hgvs: HGVS name of the variant.