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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g15180	A05	8098052	G	A	upstream_gene_variant	MODIFIER	c.-3904G>A\|	S178
2	BAA05g15180	A05	8098284	G	A	upstream_gene_variant	MODIFIER	c.-3672G>A\|	S100 S107 S148 S2 S201 S230 S250 S265 S267 S269 S286 S298 S35 S42 S47 S65 S70
3	BAA05g15180	A05	8098525	C	T	upstream_gene_variant	MODIFIER	c.-3431C>T\|	S146
4	BAA05g15180	A05	8099133	C	T	upstream_gene_variant	MODIFIER	c.-2823C>T\|	S265
5	BAA05g15180	A05	8099239	C	T	upstream_gene_variant	MODIFIER	c.-2717C>T\|	S133
6	BAA05g15180	A05	8099300	C	T	upstream_gene_variant	MODIFIER	c.-2656C>T\|	S52
7	BAA05g15180	A05	8100823	C	T	upstream_gene_variant	MODIFIER	c.-1133C>T\|	S130
8	BAA05g15180	A05	8101249	C	T	upstream_gene_variant	MODIFIER	c.-707C>T\|	S267
9	BAA05g15180	A05	8101934	G	A	upstream_gene_variant	MODIFIER	c.-22G>A\|	S32
10	BAA05g15180	A05	8103236	G	A	missense_variant	MODERATE	c.208G>A\|p.Val70Met	S276
11	BAA05g15180	A05	8103241	G	A	synonymous_variant	LOW	c.213G>A\|p.Arg71Arg	S139
12	BAA05g15180	A05	8103561	G	T	missense_variant	MODERATE	c.533G>T\|p.Cys178Phe	S80
13	BAA05g15180	A05	8103718	C	T	synonymous_variant	LOW	c.690C>T\|p.Val230Val	S213
14	BAA05g15180	A05	8103761	A	G	missense_variant	MODERATE	c.733A>G\|p.Ser245Gly	S258
15	BAA05g15180	A05	8107103	G	A	downstream_gene_variant	MODIFIER	c.*3025G>A\|	S129