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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
6751	BAA01g05570	A01	2458994	C	T	upstream_gene_variant	MODIFIER	c.-3335G>A\|	S2
6752	BAA01g05570	A01	2459687	C	T	upstream_gene_variant	MODIFIER	c.-4028G>A\|	S231
6753	BAA01g05570	A01	2460477	G	A	upstream_gene_variant	MODIFIER	c.-4818C>T\|	S262
6754	BAA01g05580	A01	2460986	G	A	upstream_gene_variant	MODIFIER	c.-4313G>A\|	S116 S118
6755	BAA01g05580	A01	2462082	G	A	upstream_gene_variant	MODIFIER	c.-3217G>A\|	S34
6756	BAA01g05580	A01	2462881	G	A	upstream_gene_variant	MODIFIER	c.-2418G>A\|	S257
6757	BAA01g05580	A01	2465555	C	T	missense_variant	MODERATE	c.257C>T\|p.Ser86Leu	S18
6758	BAA01g05580	A01	2465743	G	A	missense_variant	MODERATE	c.445G>A\|p.Ala149Thr	S95
6759	BAA01g05580	A01	2466748	C	T	downstream_gene_variant	MODIFIER	c.*868C>T\|	S133
6760	BAA01g05580	A01	2466988	C	T	downstream_gene_variant	MODIFIER	c.*1108C>T\|	S207
6761	BAA01g05590	A01	2468797	G	A	synonymous_variant	LOW	c.1816C>T\|p.Leu606Leu	S104 S52
6762	BAA01g05590	A01	2469278	C	T	synonymous_variant	LOW	c.1335G>A\|p.Gln445Gln	S126
6763	BAA01g05590	A01	2469322	T	C	missense_variant	MODERATE	c.1291A>G\|p.Met431Val	S288
6764	BAA01g05600	A01	2469466	C	T	upstream_gene_variant	MODIFIER	c.-4933C>T\|	S40 S49
6765	BAA01g05600	A01	2469492	C	T	upstream_gene_variant	MODIFIER	c.-4907C>T\|	S36
6766	BAA01g05590	A01	2469588	C	T	missense_variant	MODERATE	c.1150G>A\|p.Ala384Thr	S225 S73
6767	BAA01g05600	A01	2469720	G	A	upstream_gene_variant	MODIFIER	c.-4679G>A\|	S86
6768	BAA01g05600	A01	2469760	G	A	upstream_gene_variant	MODIFIER	c.-4639G>A\|	S172 S217
6769	BAA01g05590	A01	2470387	C	T	synonymous_variant	LOW	c.582G>A\|p.Arg194Arg	S158
6770	BAA01g05590	A01	2470421	G	A	missense_variant	MODERATE	c.548C>T\|p.Ser183Phe	S280
6771	BAA01g05590	A01	2470861	G	A	missense_variant	MODERATE	c.416C>T\|p.Thr139Ile	S242
6772	BAA01g05590	A01	2470910	C	T	missense_variant	MODERATE	c.367G>A\|p.Asp123Asn	S68
6773	BAA01g05590	A01	2471007	G	A	missense_variant	MODERATE	c.344C>T\|p.Pro115Leu	S159 S243
6774	BAA01g05590	A01	2471613	C	T	synonymous_variant	LOW	c.168G>A\|p.Glu56Glu	S120
6775	BAA01g05590	A01	2471654	C	T	missense_variant	MODERATE	c.127G>A\|p.Glu43Lys	S74

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