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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
76951	BAA01g40650	A01	26918311	C	T	upstream_gene_variant	MODIFIER	c.-3187G>A\|	S183 S198
76952	BAA01g40650	A01	26918851	C	T	upstream_gene_variant	MODIFIER	c.-3727G>A\|	S164
76953	BAA01g40650	A01	26919540	G	A	upstream_gene_variant	MODIFIER	c.-4416C>T\|	S35
76954	BAA01g40650	A01	26920027	C	T	upstream_gene_variant	MODIFIER	c.-4903G>A\|	S64
76955	BAA01g40650	A01	26920104	C	T	upstream_gene_variant	MODIFIER	c.-4980G>A\|	S301 S304
76956	BAA01g40660	A01	26920626	G	A	downstream_gene_variant	MODIFIER	c.*2971G>A\|	S189
76957	BAA01g40660	A01	26921392	G	A	downstream_gene_variant	MODIFIER	c.*3737G>A\|	S126
76958	BAA01g40660	A01	26922317	G	A	downstream_gene_variant	MODIFIER	c.*4662G>A\|	S208
76959	BAA01g40670	A01	26924335	G	A	upstream_gene_variant	MODIFIER	c.-3521G>A\|	S181
76960	BAA01g40670	A01	26924765	G	A	upstream_gene_variant	MODIFIER	c.-3091G>A\|	S152
76961	BAA01g40670	A01	26925234	G	A	upstream_gene_variant	MODIFIER	c.-2622G>A\|	S189
76962	BAA01g40670	A01	26925632	C	T	upstream_gene_variant	MODIFIER	c.-2224C>T\|	S92
76963	BAA01g40670	A01	26925699	G	A	upstream_gene_variant	MODIFIER	c.-2157G>A\|	S8
76964	BAA01g40670	A01	26927374	C	T	upstream_gene_variant	MODIFIER	c.-482C>T\|	S292
76965	BAA01g40680	A01	26928163	C	T	downstream_gene_variant	MODIFIER	c.*1536G>A\|	S25
76966	BAA01g40680	A01	26928900	C	T	downstream_gene_variant	MODIFIER	c.*799G>A\|	S146
76967	BAA01g40670	A01	26929292	C	T	missense_variant	MODERATE	c.584C>T\|p.Pro195Leu	S132 S137 S138 S215 S237 S288
76968	BAA01g40670	A01	26929472	C	T	downstream_gene_variant	MODIFIER	c.*50C>T\|	S79 S84
76969	BAA01g40690	A01	26929610	C	T	upstream_gene_variant	MODIFIER	c.-4893C>T\|	S206 S26
76970	BAA01g40680	A01	26930267	C	T	missense_variant	MODERATE	c.733G>A\|p.Glu245Lys	S127
76971	BAA01g40680	A01	26930298	G	A	synonymous_variant	LOW	c.702C>T\|p.Ala234Ala	S221
76972	BAA01g40680	A01	26930727	G	A	synonymous_variant	LOW	c.624C>T\|p.Gly208Gly	S255 S260
76973	BAA01g40680	A01	26930814	C	T	synonymous_variant	LOW	c.537G>A\|p.Glu179Glu	S267
76974	BAA01g40680	A01	26931272	C	T	missense_variant	MODERATE	c.79G>A\|p.Asp27Asn	S239
76975	BAA01g40680	A01	26931687	G	A	upstream_gene_variant	MODIFIER	c.-337C>T\|	S103

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