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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
33601	BAA01g22830	A01	11588403	G	A	upstream_gene_variant	MODIFIER	c.-4562G>A\|	S302
33602	BAA01g22830	A01	11590938	C	T	upstream_gene_variant	MODIFIER	c.-2027C>T\|	S36
33603	BAA01g22830	A01	11592562	A	T	upstream_gene_variant	MODIFIER	c.-403A>T\|	S137 S151 S175 S185 S190 S251 S27 S283 S44
33604	BAA01g22840	A01	11595169	G	A	missense_variant	MODERATE	c.314G>A\|p.Arg105Lys	S298
33605	BAA01g22840	A01	11595699	G	A	missense_variant	MODERATE	c.844G>A\|p.Val282Ile	S15 S3
33606	BAA01g22850	A01	11601626	C	T	upstream_gene_variant	MODIFIER	c.-890G>A\|	S104 S52
33607	BAA01g22850	A01	11601681	C	T	upstream_gene_variant	MODIFIER	c.-945G>A\|	S114
33608	BAA01g22850	A01	11601841	G	A	upstream_gene_variant	MODIFIER	c.-1105C>T\|	S156
33609	BAA01g22850	A01	11602843	C	T	upstream_gene_variant	MODIFIER	c.-2107G>A\|	S171
33610	BAA01g22850	A01	11603831	G	A	upstream_gene_variant	MODIFIER	c.-3095C>T\|	S83 S88
33611	BAA01g22860	A01	11606307	C	T	upstream_gene_variant	MODIFIER	c.-1369G>A\|	S267
33612	BAA01g22860	A01	11606795	G	A	upstream_gene_variant	MODIFIER	c.-1857C>T\|	S45
33613	BAA01g22860	A01	11606796	G	A	upstream_gene_variant	MODIFIER	c.-1858C>T\|	S193
33614	BAA01g22860	A01	11607181	C	A	upstream_gene_variant	MODIFIER	c.-2243G>T\|	S15 S3
33615	BAA01g22860	A01	11607248	G	A	upstream_gene_variant	MODIFIER	c.-2310C>T\|	S103
33616	BAA01g22860	A01	11607314	C	T	upstream_gene_variant	MODIFIER	c.-2376G>A\|	S177
33617	BAA01g22860	A01	11607914	G	A	upstream_gene_variant	MODIFIER	c.-2976C>T\|	S190
33618	BAA01g22860	A01	11608277	G	A	upstream_gene_variant	MODIFIER	c.-3339C>T\|	S84 S93
33619	BAA01g22860	A01	11608447	G	A	upstream_gene_variant	MODIFIER	c.-3509C>T\|	S47
33620	BAA01g22860	A01	11608676	G	A	upstream_gene_variant	MODIFIER	c.-3738C>T\|	S15 S3
33621	BAA01g22860	A01	11608740	C	T	upstream_gene_variant	MODIFIER	c.-3802G>A\|	S107
33622	BAA01g22860	A01	11609220	C	T	upstream_gene_variant	MODIFIER	c.-4282G>A\|	S47
33623	BAA01g22870	A01	11610131	G	A	upstream_gene_variant	MODIFIER	c.-442G>A\|	S297
33624	BAA01g22870	A01	11610638	G	A	synonymous_variant	LOW	c.66G>A\|p.Val22Val	S287
33625	BAA01g22870	A01	11610842	C	T	synonymous_variant	LOW	c.270C>T\|p.Pro90Pro	S112 S225 S73

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