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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g44270	A01	29424184	C	T	downstream_gene_variant	MODIFIER	c.*4960G>A\|	S15 S199 S205 S208 S209 S231 S239 S286 S296 S30 S60 S64
2	BAA01g44270	A01	29425597	C	T	downstream_gene_variant	MODIFIER	c.*3547G>A\|	S32
3	BAA01g44270	A01	29425696	A	C	downstream_gene_variant	MODIFIER	c.*3448T>G\|	S256
4	BAA01g44270	A01	29426549	C	T	downstream_gene_variant	MODIFIER	c.*2595G>A\|	S303
5	BAA01g44270	A01	29426588	C	T	downstream_gene_variant	MODIFIER	c.*2556G>A\|	S270
6	BAA01g44270	A01	29426763	A	G	downstream_gene_variant	MODIFIER	c.*2381T>C\|	S123
7	BAA01g44270	A01	29426800	G	A	downstream_gene_variant	MODIFIER	c.*2344C>T\|	S217
8	BAA01g44270	A01	29428623	C	T	downstream_gene_variant	MODIFIER	c.*521G>A\|	S241
9	BAA01g44270	A01	29428716	C	T	downstream_gene_variant	MODIFIER	c.*428G>A\|	S153 S213
10	BAA01g44270	A01	29429302	C	T	missense_variant	MODERATE	c.889G>A\|p.Ala297Thr	S279
11	BAA01g44270	A01	29429602	G	A	missense_variant	MODERATE	c.589C>T\|p.Leu197Phe	S95
12	BAA01g44270	A01	29430504	C	T	upstream_gene_variant	MODIFIER	c.-314G>A\|	S134
13	BAA01g44270	A01	29430856	C	T	upstream_gene_variant	MODIFIER	c.-666G>A\|	S178
14	BAA01g44270	A01	29433443	G	A	upstream_gene_variant	MODIFIER	c.-3253C>T\|	S176