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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
21101	BAA01g15430	A01	7440838	C	T	downstream_gene_variant	MODIFIER	c.*725C>T\|	S284
21102	BAA01g15430	A01	7441342	C	T	downstream_gene_variant	MODIFIER	c.*1229C>T\|	S19
21103	BAA01g15430	A01	7441494	C	T	downstream_gene_variant	MODIFIER	c.*1381C>T\|	S41
21104	BAA01g15430	A01	7441562	G	A	downstream_gene_variant	MODIFIER	c.*1449G>A\|	S17
21105	BAA01g15430	A01	7441619	C	T	downstream_gene_variant	MODIFIER	c.*1506C>T\|	S4
21106	BAA01g15430	A01	7442034	G	A	downstream_gene_variant	MODIFIER	c.*1921G>A\|	S155 S211
21107	BAA01g15430	A01	7442078	G	A	downstream_gene_variant	MODIFIER	c.*1965G>A\|	S17
21108	BAA01g15430	A01	7442576	C	T	downstream_gene_variant	MODIFIER	c.*2463C>T\|	S111
21109	BAA01g15430	A01	7442623	C	T	downstream_gene_variant	MODIFIER	c.*2510C>T\|	S200
21110	BAA01g15430	A01	7442959	A	C	downstream_gene_variant	MODIFIER	c.*2846A>C\|	S103 S138 S151 S165 S171 S173 S229 S233 S250 S268 S279 S289 S297 S306 S41 S86 S88
21111	BAA01g15430	A01	7442990	G	A	downstream_gene_variant	MODIFIER	c.*2877G>A\|	S252
21112	BAA01g15430	A01	7443008	G	A	downstream_gene_variant	MODIFIER	c.*2895G>A\|	S287
21113	BAA01g15430	A01	7443949	C	T	downstream_gene_variant	MODIFIER	c.*3836C>T\|	S164
21114	BAA01g15440	A01	7444821	C	T	upstream_gene_variant	MODIFIER	c.-4618C>T\|	S138
21115	BAA01g15440	A01	7445622	G	A	upstream_gene_variant	MODIFIER	c.-3817G>A\|	S192
21116	BAA01g15440	A01	7446811	G	A	upstream_gene_variant	MODIFIER	c.-2628G>A\|	S140
21117	BAA01g15440	A01	7447632	G	A	upstream_gene_variant	MODIFIER	c.-1807G>A\|	S94
21118	BAA01g15440	A01	7447822	G	A	upstream_gene_variant	MODIFIER	c.-1617G>A\|	S58
21119	BAA01g15440	A01	7447880	C	T	upstream_gene_variant	MODIFIER	c.-1559C>T\|	S226
21120	BAA01g15440	A01	7448100	C	T	upstream_gene_variant	MODIFIER	c.-1339C>T\|	S77 S82
21121	BAA01g15440	A01	7448478	G	A	upstream_gene_variant	MODIFIER	c.-961G>A\|	S297
21122	BAA01g15440	A01	7448639	G	A	upstream_gene_variant	MODIFIER	c.-800G>A\|	S149
21123	BAA01g15440	A01	7449214	C	T	upstream_gene_variant	MODIFIER	c.-225C>T\|	S10
21124	BAA01g15440	A01	7450153	G	A	missense_variant	MODERATE	c.280G>A\|p.Glu94Lys	S56
21125	BAA01g15440	A01	7450381	G	A	synonymous_variant	LOW	c.432G>A\|p.Thr144Thr	S305

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