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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g16230	A09	9381014	G	A	downstream_gene_variant	MODIFIER	c.*4493C>T\|	S152
2	BAA09g16230	A09	9381496	C	T	downstream_gene_variant	MODIFIER	c.*4011G>A\|	S211
3	BAA09g16230	A09	9381663	C	T	downstream_gene_variant	MODIFIER	c.*3844G>A\|	S263
4	BAA09g16230	A09	9382576	G	A	downstream_gene_variant	MODIFIER	c.*2931C>T\|	S240
5	BAA09g16230	A09	9384524	G	A	downstream_gene_variant	MODIFIER	c.*983C>T\|	S133 S172 S202 S217
6	BAA09g16230	A09	9385542	C	T	missense_variant	MODERATE	c.712G>A\|p.Glu238Lys	S60
7	BAA09g16230	A09	9385581	G	A	missense_variant	MODERATE	c.673C>T\|p.Pro225Ser	S238
8	BAA09g16230	A09	9385619	C	T	missense_variant	MODERATE	c.635G>A\|p.Gly212Asp	S250
9	BAA09g16230	A09	9385903	C	T	missense_variant	MODERATE	c.351G>A\|p.Met117Ile	S270
10	BAA09g16230	A09	9386801	G	A	upstream_gene_variant	MODIFIER	c.-548C>T\|	S245
11	BAA09g16230	A09	9389545	C	T	upstream_gene_variant	MODIFIER	c.-3292G>A\|	S159 S187 S188 S243 S276 S299
12	BAA09g16230	A09	9389683	C	T	upstream_gene_variant	MODIFIER	c.-3430G>A\|	S28
13	BAA09g16230	A09	9390266	G	A	upstream_gene_variant	MODIFIER	c.-4013C>T\|	S142
14	BAA09g16230	A09	9390991	G	A	upstream_gene_variant	MODIFIER	c.-4738C>T\|	S97