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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
119301	BAA10g11420-BAA10g11430	A10	12994676	G	A	intergenic_region	MODIFIER	n.12994676G>A\|	S65
119302	BAA10g11420-BAA10g11430	A10	12995222	C	T	intergenic_region	MODIFIER	n.12995222C>T\|	S153 S213 S293
119303	BAA10g11420-BAA10g11430	A10	12995841	C	T	intergenic_region	MODIFIER	n.12995841C>T\|	S153 S213
119304	BAA10g11420-BAA10g11430	A10	12996611	G	A	intergenic_region	MODIFIER	n.12996611G>A\|	S157 S163
119305	BAA10g11420-BAA10g11430	A10	12998360	T	A	intergenic_region	MODIFIER	n.12998360T>A\|	S168
119306	BAA10g11420-BAA10g11430	A10	13002401	C	T	intergenic_region	MODIFIER	n.13002401C>T\|	S20
119307	BAA10g11420-BAA10g11430	A10	13005761	G	A	intergenic_region	MODIFIER	n.13005761G>A\|	S251
119308	BAA10g11420-BAA10g11430	A10	13006738	C	T	intergenic_region	MODIFIER	n.13006738C>T\|	S138
119309	BAA10g11420-BAA10g11430	A10	13009222	C	T	intergenic_region	MODIFIER	n.13009222C>T\|	S42
119310	BAA10g11420-BAA10g11430	A10	13010952	G	A	intergenic_region	MODIFIER	n.13010952G>A\|	S159 S243
119311	BAA10g11430	A10	13012170	G	A	downstream_gene_variant	MODIFIER	c.*4915C>T\|	S136
119312	BAA10g11430	A10	13013189	G	A	downstream_gene_variant	MODIFIER	c.*3896C>T\|	S290
119313	BAA10g11430	A10	13013396	G	A	downstream_gene_variant	MODIFIER	c.*3689C>T\|	S245 S273
119314	BAA10g11430	A10	13014352	C	T	downstream_gene_variant	MODIFIER	c.*2733G>A\|	S34
119315	BAA10g11430	A10	13014372	G	A	downstream_gene_variant	MODIFIER	c.*2713C>T\|	S159 S187 S188 S243 S276
119316	BAA10g11430	A10	13014533	G	A	downstream_gene_variant	MODIFIER	c.*2552C>T\|	S192
119317	BAA10g11430	A10	13014917	C	T	downstream_gene_variant	MODIFIER	c.*2168G>A\|	S301 S304
119318	BAA10g11430	A10	13015082	C	T	downstream_gene_variant	MODIFIER	c.*2003G>A\|	S40 S49
119319	BAA10g11430	A10	13015288	C	T	downstream_gene_variant	MODIFIER	c.*1797G>A\|	S236
119320	BAA10g11430	A10	13015323	G	C	downstream_gene_variant	MODIFIER	c.*1762C>G\|	S175
119321	BAA10g11430	A10	13015435	C	T	downstream_gene_variant	MODIFIER	c.*1650G>A\|	S195
119322	BAA10g11430	A10	13015478	C	T	downstream_gene_variant	MODIFIER	c.*1607G>A\|	S116
119323	BAA10g11440	A10	13017074	G	A	upstream_gene_variant	MODIFIER	c.-4483G>A\|	S290
119324	BAA10g11440	A10	13017382	C	T	upstream_gene_variant	MODIFIER	c.-4175C>T\|	S186
119325	BAA10g11430	A10	13017628	G	A	missense_variant	MODERATE	c.223C>T\|p.His75Tyr	S94

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