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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
178951	BAA02g19660	A02	10225254	C	T	upstream_gene_variant	MODIFIER	c.-2834G>A\|	S262
178952	BAA02g19660	A02	10225283	G	C	upstream_gene_variant	MODIFIER	c.-2863C>G\|	S1 S105 S108 S119 S128 S149 S158 S183 S193 S20 S217 S218 S226 S27 S283 S290 S45 S53 S56
178953	BAA02g19660	A02	10225600	A	G	upstream_gene_variant	MODIFIER	c.-3180T>C\|
178954	BAA02g19660	A02	10225629	C	T	upstream_gene_variant	MODIFIER	c.-3209G>A\|	S158
178955	BAA02g19660	A02	10226197	G	A	upstream_gene_variant	MODIFIER	c.-3777C>T\|	S306 S308
178956	BAA02g19660	A02	10226395	G	A	upstream_gene_variant	MODIFIER	c.-3975C>T\|	S256
178957	BAA02g19660	A02	10226601	C	T	upstream_gene_variant	MODIFIER	c.-4181G>A\|	S127
178958	BAA02g19660	A02	10226804	C	T	upstream_gene_variant	MODIFIER	c.-4384G>A\|	S104 S52
178959	BAA02g19660	A02	10227070	G	A	upstream_gene_variant	MODIFIER	c.-4650C>T\|	S288
178960	BAA02g19670	A02	10228652	G	A	downstream_gene_variant	MODIFIER	c.*3912C>T\|	S223
178961	BAA02g19670	A02	10228784	G	A	downstream_gene_variant	MODIFIER	c.*3780C>T\|	S263
178962	BAA02g19670	A02	10229353	C	T	downstream_gene_variant	MODIFIER	c.*3211G>A\|	S267
178963	BAA02g19670	A02	10230854	C	T	downstream_gene_variant	MODIFIER	c.*1710G>A\|	S105 S106
178964	BAA02g19670	A02	10233232	G	A	upstream_gene_variant	MODIFIER	c.-225C>T\|	S202
178965	BAA02g19670	A02	10233337	G	A	upstream_gene_variant	MODIFIER	c.-330C>T\|	S280
178966	BAA02g19670	A02	10234327	G	A	upstream_gene_variant	MODIFIER	c.-1320C>T\|	S291
178967	BAA02g19670	A02	10235335	G	A	upstream_gene_variant	MODIFIER	c.-2328C>T\|	S235
178968	BAA02g19670	A02	10235522	C	T	upstream_gene_variant	MODIFIER	c.-2515G>A\|	S266
178969	BAA02g19670	A02	10237570	C	T	upstream_gene_variant	MODIFIER	c.-4563G>A\|	S216 S241 S265
178970	BAA02g19680	A02	10238712	C	T	upstream_gene_variant	MODIFIER	c.-521C>T\|	S112
178971	BAA02g19680	A02	10239307	C	T	synonymous_variant	LOW	c.75C>T\|p.Leu25Leu	S203
178972	BAA02g19680	A02	10239976	G	A	stop_gained	HIGH	c.744G>A\|p.Trp248*	S279
178973	BAA02g19680	A02	10239978	G	A	missense_variant	MODERATE	c.746G>A\|p.Arg249Lys	S125
178974	BAA02g19680	A02	10240586	G	A	downstream_gene_variant	MODIFIER	c.*403G>A\|	S293
178975	BAA02g19680	A02	10241436	C	T	downstream_gene_variant	MODIFIER	c.*1253C>T\|	S224

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