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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
39001	BAA01g25080-BAA01g25090	A01	13444784	C	T	intergenic_region	MODIFIER	n.13444784C>T\|	S289 S290
39002	BAA01g25080-BAA01g25090	A01	13444984	C	T	intergenic_region	MODIFIER	n.13444984C>T\|	S153
39003	BAA01g25090	A01	13445361	G	A	downstream_gene_variant	MODIFIER	c.*4956C>T\|	S187
39004	BAA01g25090	A01	13445460	G	A	downstream_gene_variant	MODIFIER	c.*4857C>T\|	S119
39005	BAA01g25090	A01	13445695	C	T	downstream_gene_variant	MODIFIER	c.*4622G>A\|	S162
39006	BAA01g25090	A01	13445928	G	A	downstream_gene_variant	MODIFIER	c.*4389C>T\|	S56
39007	BAA01g25090	A01	13446213	G	A	downstream_gene_variant	MODIFIER	c.*4104C>T\|	S73 S91
39008	BAA01g25090	A01	13446680	G	A	downstream_gene_variant	MODIFIER	c.*3637C>T\|	S63
39009	BAA01g25090	A01	13447581	C	T	downstream_gene_variant	MODIFIER	c.*2736G>A\|	S81 S85
39010	BAA01g25090	A01	13449559	C	T	downstream_gene_variant	MODIFIER	c.*758G>A\|	S104 S52
39011	BAA01g25090	A01	13450923	C	T	splice_region_variant&synonymous_variant	LOW	c.117G>A\|p.Lys39Lys	S19
39012	BAA01g25090	A01	13450932	G	A	synonymous_variant	LOW	c.108C>T\|p.Asp36Asp	S244
39013	BAA01g25090	A01	13452381	C	T	upstream_gene_variant	MODIFIER	c.-1342G>A\|	S167
39014	BAA01g25090	A01	13452681	C	T	upstream_gene_variant	MODIFIER	c.-1642G>A\|	S255
39015	BAA01g25090	A01	13453370	C	T	upstream_gene_variant	MODIFIER	c.-2331G>A\|	S82 S92
39016	BAA01g25090	A01	13453887	C	T	upstream_gene_variant	MODIFIER	c.-2848G>A\|	S251
39017	BAA01g25090-BAA01g25100	A01	13458030	G	A	intergenic_region	MODIFIER	n.13458030G>A\|	S199
39018	BAA01g25090-BAA01g25100	A01	13459499	C	T	intergenic_region	MODIFIER	n.13459499C>T\|	S295
39019	BAA01g25090-BAA01g25100	A01	13459701	G	A	intergenic_region	MODIFIER	n.13459701G>A\|	S38
39020	BAA01g25090-BAA01g25100	A01	13463544	G	A	intergenic_region	MODIFIER	n.13463544G>A\|	S105 S106
39021	BAA01g25090-BAA01g25100	A01	13465377	G	A	intergenic_region	MODIFIER	n.13465377G>A\|	S298
39022	BAA01g25100	A01	13467245	G	A	downstream_gene_variant	MODIFIER	c.*4349C>T\|	S197
39023	BAA01g25100	A01	13467271	C	T	downstream_gene_variant	MODIFIER	c.*4323G>A\|	S19
39024	BAA01g25100	A01	13473768	C	T	upstream_gene_variant	MODIFIER	c.-1215G>A\|	S180
39025	BAA01g25100	A01	13474389	C	T	upstream_gene_variant	MODIFIER	c.-1836G>A\|	S136

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