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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
180051	BAA02g20150	A02	10628400	C	T	upstream_gene_variant	MODIFIER	c.-3729G>A\|	S135
180052	BAA02g20150	A02	10629286	C	T	upstream_gene_variant	MODIFIER	c.-4615G>A\|	S38
180053	BAA02g20150	A02	10629317	G	A	upstream_gene_variant	MODIFIER	c.-4646C>T\|	S229
180054	BAA02g20150	A02	10629357	G	T	upstream_gene_variant	MODIFIER	c.-4686C>A\|	S199
180055	BAA02g20150	A02	10629499	C	T	upstream_gene_variant	MODIFIER	c.-4828G>A\|	S75 S81
180056	BAA02g20160	A02	10629835	C	T	upstream_gene_variant	MODIFIER	c.-2913G>A\|	S211 S227
180057	BAA02g20160	A02	10630303	C	T	upstream_gene_variant	MODIFIER	c.-3381G>A\|	S6
180058	BAA02g20160	A02	10631106	C	T	upstream_gene_variant	MODIFIER	c.-4184G>A\|	S159 S188 S243 S276 S298 S299
180059	BAA02g20160-BAA02g20170	A02	10632918	A	T	intergenic_region	MODIFIER	n.10632918A>T\|	S272
180060	BAA02g20160-BAA02g20170	A02	10635806	G	A	intergenic_region	MODIFIER	n.10635806G>A\|	S291
180061	BAA02g20170	A02	10636229	C	T	upstream_gene_variant	MODIFIER	c.-4985C>T\|	S79
180062	BAA02g20170	A02	10636858	C	T	upstream_gene_variant	MODIFIER	c.-4356C>T\|	S67
180063	BAA02g20170	A02	10637158	G	A	upstream_gene_variant	MODIFIER	c.-4056G>A\|	S272
180064	BAA02g20170	A02	10637277	C	T	upstream_gene_variant	MODIFIER	c.-3937C>T\|	S216
180065	BAA02g20170	A02	10637531	C	T	upstream_gene_variant	MODIFIER	c.-3683C>T\|	S105 S106
180066	BAA02g20170	A02	10637558	C	T	upstream_gene_variant	MODIFIER	c.-3656C>T\|	S165 S211 S227
180067	BAA02g20170	A02	10640099	G	A	upstream_gene_variant	MODIFIER	c.-1115G>A\|	S190
180068	BAA02g20170	A02	10640546	C	T	upstream_gene_variant	MODIFIER	c.-668C>T\|	S25
180069	BAA02g20170	A02	10642534	C	T	intron_variant	MODIFIER	c.801+77C>T\|	S212
180070	BAA02g20170	A02	10644085	C	T	intron_variant	MODIFIER	c.1329+35C>T\|	S121
180071	BAA02g20170	A02	10648309	G	A	synonymous_variant	LOW	c.3564G>A\|p.Arg1188Arg	S298
180072	BAA02g20180	A02	10648707	C	T	downstream_gene_variant	MODIFIER	c.*2374G>A\|	S77 S82
180073	BAA02g20170	A02	10649639	G	A	missense_variant	MODERATE	c.4409G>A\|p.Arg1470Lys	S155 S211
180074	BAA02g20170	A02	10650698	C	T	downstream_gene_variant	MODIFIER	c.*75C>T\|	S25
180075	BAA02g20170	A02	10652158	C	T	downstream_gene_variant	MODIFIER	c.*1535C>T\|	S185

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