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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
45751	BAA01g27280-BAA01g27290	A01	15695735	C	A	intergenic_region	MODIFIER	n.15695735C>A\|	S172 S217
45752	BAA01g27280-BAA01g27290	A01	15699865	C	T	intergenic_region	MODIFIER	n.15699865C>T\|	S125
45753	BAA01g27280-BAA01g27290	A01	15700787	C	T	intergenic_region	MODIFIER	n.15700787C>T\|	S153
45754	BAA01g27290	A01	15721093	G	A	upstream_gene_variant	MODIFIER	c.-3494G>A\|	S80
45755	BAA01g27290	A01	15721593	C	T	upstream_gene_variant	MODIFIER	c.-2994C>T\|	S250
45756	BAA01g27290	A01	15722088	G	A	upstream_gene_variant	MODIFIER	c.-2499G>A\|	S72
45757	BAA01g27290	A01	15722268	C	T	upstream_gene_variant	MODIFIER	c.-2319C>T\|	S259
45758	BAA01g27290	A01	15723315	C	T	upstream_gene_variant	MODIFIER	c.-1272C>T\|	S151 S166 S263
45759	BAA01g27290	A01	15724027	C	T	upstream_gene_variant	MODIFIER	c.-560C>T\|	S120
45760	BAA01g27290	A01	15724732	A	G	missense_variant	MODERATE	c.146A>G\|p.Gln49Arg	S131
45761	BAA01g27300	A01	15724880	G	A	downstream_gene_variant	MODIFIER	c.*2509C>T\|	S292
45762	BAA01g27300	A01	15725107	C	T	downstream_gene_variant	MODIFIER	c.*2282G>A\|	S286
45763	BAA01g27290	A01	15726222	C	T	downstream_gene_variant	MODIFIER	c.*15C>T\|	S61
45764	BAA01g27290	A01	15726457	G	A	downstream_gene_variant	MODIFIER	c.*250G>A\|	S5
45765	BAA01g27290	A01	15727157	G	A	downstream_gene_variant	MODIFIER	c.*950G>A\|	S56
45766	BAA01g27290	A01	15727356	C	T	downstream_gene_variant	MODIFIER	c.*1149C>T\|	S30 S31
45767	BAA01g27290	A01	15729791	C	T	downstream_gene_variant	MODIFIER	c.*3584C>T\|	S282
45768	BAA01g27290	A01	15729914	G	A	downstream_gene_variant	MODIFIER	c.*3707G>A\|	S271
45769	BAA01g27290	A01	15730151	C	T	downstream_gene_variant	MODIFIER	c.*3944C>T\|	S128
45770	BAA01g27290	A01	15730448	C	T	downstream_gene_variant	MODIFIER	c.*4241C>T\|	S132 S137 S215 S89
45771	BAA01g27290	A01	15730700	G	A	downstream_gene_variant	MODIFIER	c.*4493G>A\|	S105 S106
45772	BAA01g27300	A01	15731594	G	A	intron_variant	MODIFIER	c.266-4108C>T\|	S306 S308
45773	BAA01g27300	A01	15731700	C	T	intron_variant	MODIFIER	c.266-4214G>A\|	S289 S290
45774	BAA01g27300	A01	15731882	C	T	intron_variant	MODIFIER	c.266-4396G>A\|	S111
45775	BAA01g27300	A01	15733154	C	T	intron_variant	MODIFIER	c.265+3479G>A\|	S47

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