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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g38460	A02	32760766	G	A	upstream_gene_variant	MODIFIER	c.-1877G>A\|	S174 S27
2	BAA02g38460	A02	32760930	G	A	upstream_gene_variant	MODIFIER	c.-1713G>A\|	S292
3	BAA02g38460	A02	32761203	G	A	upstream_gene_variant	MODIFIER	c.-1440G>A\|	S279
4	BAA02g38460	A02	32761821	G	A	upstream_gene_variant	MODIFIER	c.-822G>A\|	S133
5	BAA02g38460	A02	32761996	G	T	upstream_gene_variant	MODIFIER	c.-647G>T\|	S124 S13 S158 S171 S186 S221 S282 S38 S47 S71
6	BAA02g38460	A02	32762719	C	T	missense_variant	MODERATE	c.77C>T\|p.Ser26Leu	S135
7	BAA02g38460	A02	32762942	G	A	synonymous_variant	LOW	c.300G>A\|p.Gln100Gln	S50
8	BAA02g38460	A02	32762981	G	A	synonymous_variant	LOW	c.339G>A\|p.Lys113Lys	S295
9	BAA02g38460	A02	32763122	G	A	synonymous_variant	LOW	c.480G>A\|p.Leu160Leu	S90
10	BAA02g38460	A02	32763786	G	A	missense_variant	MODERATE	c.1144G>A\|p.Asp382Asn	S186
11	BAA02g38460	A02	32767262	C	T	downstream_gene_variant	MODIFIER	c.*3468C>T\|	S296
12	BAA02g38460	A02	32767773	G	A	downstream_gene_variant	MODIFIER	c.*3979G>A\|	S13
13	BAA02g38460	A02	32767914	C	T	downstream_gene_variant	MODIFIER	c.*4120C>T\|	S100