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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
177601	BAA02g18880-BAA02g18890	A02	9760984	G	A	intergenic_region	MODIFIER	n.9760984G>A\|	S177
177602	BAA02g18880-BAA02g18890	A02	9761098	G	A	intergenic_region	MODIFIER	n.9761098G>A\|	S189
177603	BAA02g18890	A02	9762224	C	T	upstream_gene_variant	MODIFIER	c.-4120C>T\|	S255
177604	BAA02g18890	A02	9762675	G	A	upstream_gene_variant	MODIFIER	c.-3669G>A\|	S62
177605	BAA02g18890	A02	9765061	G	A	upstream_gene_variant	MODIFIER	c.-1283G>A\|	S122 S221
177606	BAA02g18890	A02	9765783	C	T	upstream_gene_variant	MODIFIER	c.-561C>T\|	S105 S106
177607	BAA02g18890	A02	9766214	G	A	upstream_gene_variant	MODIFIER	c.-130G>A\|	S296
177608	BAA02g18890	A02	9767055	C	T	intron_variant	MODIFIER	c.403-109C>T\|	S241
177609	BAA02g18890	A02	9768681	G	A	downstream_gene_variant	MODIFIER	c.*786G>A\|	S95
177610	BAA02g18890	A02	9768887	C	T	downstream_gene_variant	MODIFIER	c.*992C>T\|	S140
177611	BAA02g18890	A02	9768943	C	T	downstream_gene_variant	MODIFIER	c.*1048C>T\|	S181 S217 S248 S56
177612	BAA02g18890	A02	9769040	G	A	downstream_gene_variant	MODIFIER	c.*1145G>A\|	S17
177613	BAA02g18890	A02	9769455	G	A	downstream_gene_variant	MODIFIER	c.*1560G>A\|	S45
177614	BAA02g18890	A02	9769614	G	A	downstream_gene_variant	MODIFIER	c.*1719G>A\|	S45
177615	BAA02g18890	A02	9769790	G	A	downstream_gene_variant	MODIFIER	c.*1895G>A\|	S110
177616	BAA02g18890	A02	9769897	C	T	downstream_gene_variant	MODIFIER	c.*2002C>T\|	S234
177617	BAA02g18890	A02	9770294	G	A	downstream_gene_variant	MODIFIER	c.*2399G>A\|	S259
177618	BAA02g18900	A02	9770681	G	T	upstream_gene_variant	MODIFIER	c.-4837G>T\|	S118 S148 S157 S163 S210 S218 S249 S267 S269 S295 S30 S31 S43 S54
177619	BAA02g18900	A02	9770792	G	A	upstream_gene_variant	MODIFIER	c.-4726G>A\|	S162
177620	BAA02g18900	A02	9771061	G	A	upstream_gene_variant	MODIFIER	c.-4457G>A\|	S264
177621	BAA02g18900	A02	9771168	G	A	upstream_gene_variant	MODIFIER	c.-4350G>A\|	S187
177622	BAA02g18900	A02	9771506	G	A	upstream_gene_variant	MODIFIER	c.-4012G>A\|	S146
177623	BAA02g18900	A02	9772221	C	T	upstream_gene_variant	MODIFIER	c.-3297C>T\|	S292
177624	BAA02g18900	A02	9772271	G	A	upstream_gene_variant	MODIFIER	c.-3247G>A\|	S259
177625	BAA02g18900	A02	9772914	G	A	upstream_gene_variant	MODIFIER	c.-2604G>A\|	S193

Users can query the SNP information according to the gene ID.