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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g46200	A02	37632389	C	T	upstream_gene_variant	MODIFIER	c.-3593C>T\|	S63
2	BAA02g46200	A02	37632421	C	T	upstream_gene_variant	MODIFIER	c.-3561C>T\|	S234
3	BAA02g46200	A02	37633972	G	A	upstream_gene_variant	MODIFIER	c.-2010G>A\|	S113
4	BAA02g46200	A02	37634188	C	T	upstream_gene_variant	MODIFIER	c.-1794C>T\|	S170
5	BAA02g46200	A02	37634852	T	A	upstream_gene_variant	MODIFIER	c.-1130T>A\|	S60
6	BAA02g46200	A02	37635253	G	A	upstream_gene_variant	MODIFIER	c.-729G>A\|	S62
7	BAA02g46200	A02	37635362	G	A	upstream_gene_variant	MODIFIER	c.-620G>A\|	S103
8	BAA02g46200	A02	37635593	C	T	upstream_gene_variant	MODIFIER	c.-389C>T\|	S159 S243
9	BAA02g46200	A02	37635867	C	T	upstream_gene_variant	MODIFIER	c.-115C>T\|	S1 S90
10	BAA02g46200	A02	37637007	G	A	synonymous_variant	LOW	c.282G>A\|p.Gly94Gly	S287
11	BAA02g46200	A02	37637804	C	T	missense_variant	MODERATE	c.782C>T\|p.Ala261Val	S32
12	BAA02g46200	A02	37637922	T	G	missense_variant	MODERATE	c.826T>G\|p.Phe276Val	S160 S180 S249 S269 S38 S41 S48
13	BAA02g46200	A02	37638251	G	A	splice_region_variant&intron_variant	LOW	c.991-6G>A\|	S261
14	BAA02g46200	A02	37638316	G	A	splice_donor_variant&intron_variant	HIGH	c.1049+1G>A\|	S132 S137 S215 S89
15	BAA02g46200	A02	37642936	C	T	downstream_gene_variant	MODIFIER	c.*3930C>T\|	S255