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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
177051	BAA02g18660	A02	9558549	G	A	upstream_gene_variant	MODIFIER	c.-3139C>T\|	S43
177052	BAA02g18660	A02	9558591	C	T	upstream_gene_variant	MODIFIER	c.-3181G>A\|	S63
177053	BAA02g18660	A02	9558630	G	A	upstream_gene_variant	MODIFIER	c.-3220C>T\|	S162
177054	BAA02g18660	A02	9558719	C	T	upstream_gene_variant	MODIFIER	c.-3309G>A\|	S25
177055	BAA02g18660	A02	9559354	C	T	upstream_gene_variant	MODIFIER	c.-3944G>A\|	S46
177056	BAA02g18660	A02	9559865	C	T	upstream_gene_variant	MODIFIER	c.-4455G>A\|	S234
177057	BAA02g18670	A02	9562232	G	T	upstream_gene_variant	MODIFIER	c.-2061G>T\|	S11 S14 S17 S184 S185 S203 S218 S224 S267 S268 S271 S272 S273 S40 S49
177058	BAA02g18670	A02	9562363	G	A	upstream_gene_variant	MODIFIER	c.-1930G>A\|	S206 S26
177059	BAA02g18670	A02	9562673	G	A	upstream_gene_variant	MODIFIER	c.-1620G>A\|	S48
177060	BAA02g18670	A02	9562750	G	A	upstream_gene_variant	MODIFIER	c.-1543G>A\|	S229
177061	BAA02g18670	A02	9562871	C	T	upstream_gene_variant	MODIFIER	c.-1422C>T\|	S135
177062	BAA02g18670	A02	9562905	G	A	upstream_gene_variant	MODIFIER	c.-1388G>A\|	S56
177063	BAA02g18670	A02	9563350	G	A	upstream_gene_variant	MODIFIER	c.-943G>A\|	S203
177064	BAA02g18670	A02	9563419	G	A	upstream_gene_variant	MODIFIER	c.-874G>A\|	S228
177065	BAA02g18670	A02	9563504	G	A	upstream_gene_variant	MODIFIER	c.-789G>A\|	S238
177066	BAA02g18670	A02	9563922	G	A	upstream_gene_variant	MODIFIER	c.-371G>A\|	S251
177067	BAA02g18670	A02	9565063	G	A	downstream_gene_variant	MODIFIER	c.*486G>A\|	S144
177068	BAA02g18680	A02	9565667	C	T	missense_variant	MODERATE	c.1318G>A\|p.Glu440Lys	S244
177069	BAA02g18670	A02	9566426	G	A	downstream_gene_variant	MODIFIER	c.*1849G>A\|	S169 S297
177070	BAA02g18670	A02	9566463	C	T	downstream_gene_variant	MODIFIER	c.*1886C>T\|	S183 S198
177071	BAA02g18670	A02	9568050	C	T	downstream_gene_variant	MODIFIER	c.*3473C>T\|	S241
177072	BAA02g18670	A02	9569223	C	T	downstream_gene_variant	MODIFIER	c.*4646C>T\|	S140
177073	BAA02g18670	A02	9569317	G	A	downstream_gene_variant	MODIFIER	c.*4740G>A\|	S11
177074	BAA02g18680	A02	9569847	G	A	intron_variant	MODIFIER	c.1131+76C>T\|	S282
177075	BAA02g18680	A02	9570071	C	T	missense_variant	MODERATE	c.983G>A\|p.Gly328Asp	S278

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