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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
115151	BAA10g09620	A10	11547294	C	T	upstream_gene_variant	MODIFIER	c.-1189G>A\|	S193
115152	BAA10g09620	A10	11548941	G	A	upstream_gene_variant	MODIFIER	c.-2836C>T\|	S127
115153	BAA10g09620	A10	11550307	G	A	upstream_gene_variant	MODIFIER	c.-4202C>T\|	S13
115154	BAA10g09620-BAA10g09630	A10	11551907	G	A	intergenic_region	MODIFIER	n.11551907G>A\|	S90
115155	BAA10g09620-BAA10g09630	A10	11552123	C	A	intergenic_region	MODIFIER	n.11552123C>A\|	S114 S132 S150 S169 S198 S207 S23 S249 S257 S261 S3 S51 S59 S64 S8 S85
115156	BAA10g09620-BAA10g09630	A10	11552158	G	A	intergenic_region	MODIFIER	n.11552158G>A\|	S160
115157	BAA10g09630	A10	11553183	C	T	downstream_gene_variant	MODIFIER	c.*4896G>A\|	S113
115158	BAA10g09630	A10	11553810	C	T	downstream_gene_variant	MODIFIER	c.*4269G>A\|	S25
115159	BAA10g09630	A10	11554252	C	T	downstream_gene_variant	MODIFIER	c.*3827G>A\|	S10
115160	BAA10g09630	A10	11554608	C	T	downstream_gene_variant	MODIFIER	c.*3471G>A\|	S183
115161	BAA10g09630	A10	11554826	G	A	downstream_gene_variant	MODIFIER	c.*3253C>T\|	S71
115162	BAA10g09630	A10	11554870	G	A	downstream_gene_variant	MODIFIER	c.*3209C>T\|	S234
115163	BAA10g09630	A10	11554958	C	T	downstream_gene_variant	MODIFIER	c.*3121G>A\|	S6
115164	BAA10g09630	A10	11555314	G	A	downstream_gene_variant	MODIFIER	c.*2765C>T\|	S289
115165	BAA10g09630	A10	11555678	G	A	downstream_gene_variant	MODIFIER	c.*2401C>T\|	S295
115166	BAA10g09630	A10	11555776	G	A	downstream_gene_variant	MODIFIER	c.*2303C>T\|	S125
115167	BAA10g09630	A10	11556062	C	T	downstream_gene_variant	MODIFIER	c.*2017G>A\|	S268
115168	BAA10g09630	A10	11557280	C	T	downstream_gene_variant	MODIFIER	c.*799G>A\|	S142
115169	BAA10g09630	A10	11558426	C	T	missense_variant	MODERATE	c.583G>A\|p.Gly195Arg	S242
115170	BAA10g09630	A10	11558676	G	A	synonymous_variant	LOW	c.459C>T\|p.Phe153Phe	S55
115171	BAA10g09630	A10	11558804	G	A	missense_variant	MODERATE	c.415C>T\|p.Arg139Cys	S219
115172	BAA10g09640	A10	11558918	C	T	upstream_gene_variant	MODIFIER	c.-4938C>T\|	S40 S49
115173	BAA10g09640	A10	11560356	G	A	upstream_gene_variant	MODIFIER	c.-3500G>A\|	S138
115174	BAA10g09630	A10	11560897	C	T	upstream_gene_variant	MODIFIER	c.-67G>A\|	S225
115175	BAA10g09630	A10	11561284	C	T	upstream_gene_variant	MODIFIER	c.-454G>A\|	S37

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