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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g41070	A02	34476936	C	T	upstream_gene_variant	MODIFIER	c.-4892C>T\|	S48
2	BAA02g41070	A02	34477852	T	A	upstream_gene_variant	MODIFIER	c.-3976T>A\|	S104 S105 S106 S112 S208 S308 S53 S7 S80 S88 S89 S93 S95 S99
3	BAA02g41070	A02	34478298	G	A	upstream_gene_variant	MODIFIER	c.-3530G>A\|	S259
4	BAA02g41070	A02	34478649	G	A	upstream_gene_variant	MODIFIER	c.-3179G>A\|	S71
5	BAA02g41070	A02	34479351	C	T	upstream_gene_variant	MODIFIER	c.-2477C>T\|	S272
6	BAA02g41070	A02	34480294	G	A	upstream_gene_variant	MODIFIER	c.-1534G>A\|	S278
7	BAA02g41070	A02	34481465	C	T	upstream_gene_variant	MODIFIER	c.-363C>T\|	S192
8	BAA02g41070	A02	34481937	G	A	missense_variant	MODERATE	c.110G>A\|p.Gly37Glu	S161
9	BAA02g41070	A02	34482007	C	T	synonymous_variant	LOW	c.180C>T\|p.Asn60Asn	S117
10	BAA02g41070	A02	34482168	G	A	missense_variant	MODERATE	c.247G>A\|p.Asp83Asn	S84 S93
11	BAA02g41070	A02	34482971	G	A	missense_variant	MODERATE	c.659G>A\|p.Gly220Glu	S183 S238
12	BAA02g41070	A02	34482995	C	T	intron_variant	MODIFIER	c.666+17C>T\|	S18
13	BAA02g41070	A02	34484831	C	T	downstream_gene_variant	MODIFIER	c.*331C>T\|	S104 S52
14	BAA02g41070	A02	34485834	C	T	downstream_gene_variant	MODIFIER	c.*1334C>T\|	S42
15	BAA02g41070	A02	34486003	G	A	downstream_gene_variant	MODIFIER	c.*1503G>A\|	S204
16	BAA02g41070	A02	34486200	C	T	downstream_gene_variant	MODIFIER	c.*1700C>T\|	S47
17	BAA02g41070	A02	34486204	G	A	downstream_gene_variant	MODIFIER	c.*1704G>A\|	S298
18	BAA02g41070	A02	34486225	G	A	downstream_gene_variant	MODIFIER	c.*1725G>A\|	S224
19	BAA02g41070	A02	34486777	G	A	downstream_gene_variant	MODIFIER	c.*2277G>A\|	S69