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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g39490	A02	33543896	G	A	upstream_gene_variant	MODIFIER	c.-4482G>A\|	S28
2	BAA02g39490	A02	33547231	C	T	upstream_gene_variant	MODIFIER	c.-1147C>T\|	S216
3	BAA02g39490	A02	33547549	G	A	upstream_gene_variant	MODIFIER	c.-829G>A\|	S217 S248
4	BAA02g39490	A02	33547564	C	T	upstream_gene_variant	MODIFIER	c.-814C>T\|	S246
5	BAA02g39490	A02	33547649	G	A	upstream_gene_variant	MODIFIER	c.-729G>A\|	S281
6	BAA02g39490	A02	33547905	G	A	upstream_gene_variant	MODIFIER	c.-473G>A\|	S221
7	BAA02g39490	A02	33548069	G	A	upstream_gene_variant	MODIFIER	c.-309G>A\|	S276
8	BAA02g39490	A02	33548724	A	C	missense_variant	MODERATE	c.347A>C\|p.Tyr116Ser	S1 S122 S129 S135 S159 S202 S23 S264 S46 S64 S91
9	BAA02g39490	A02	33550358	G	A	downstream_gene_variant	MODIFIER	c.*1252G>A\|	S153 S213
10	BAA02g39490	A02	33550743	G	A	downstream_gene_variant	MODIFIER	c.*1637G>A\|	S72 S78
11	BAA02g39490	A02	33551436	C	T	downstream_gene_variant	MODIFIER	c.*2330C>T\|	S301 S304
12	BAA02g39490	A02	33551709	G	A	downstream_gene_variant	MODIFIER	c.*2603G>A\|	S111
13	BAA02g39490	A02	33552723	C	T	downstream_gene_variant	MODIFIER	c.*3617C>T\|	S157 S163
14	BAA02g39490	A02	33553051	C	T	downstream_gene_variant	MODIFIER	c.*3945C>T\|	S68