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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
83351	BAA01g44220	A01	29308681	G	A	upstream_gene_variant	MODIFIER	c.-4359C>T\|	S100
83352	BAA01g44220	A01	29308728	G	A	upstream_gene_variant	MODIFIER	c.-4406C>T\|	S172 S217
83353	BAA01g44220	A01	29308904	C	T	upstream_gene_variant	MODIFIER	c.-4582G>A\|	S57
83354	BAA01g44250	A01	29309209	G	A	missense_variant	MODERATE	c.286G>A\|p.Glu96Lys	S209
83355	BAA01g44230	A01	29309983	G	A	upstream_gene_variant	MODIFIER	c.-3486C>T\|	S182
83356	BAA01g44240	A01	29312017	G	A	downstream_gene_variant	MODIFIER	c.*4820G>A\|	S33
83357	BAA01g44250	A01	29312300	C	T	missense_variant	MODERATE	c.1054C>T\|p.Leu352Phe	S191
83358	BAA01g44250	A01	29312514	C	T	missense_variant	MODERATE	c.1136C>T\|p.Thr379Ile	S231
83359	BAA01g44250	A01	29312896	G	A	missense_variant	MODERATE	c.1295G>A\|p.Arg432Gln	S209
83360	BAA01g44260	A01	29313259	C	T	downstream_gene_variant	MODIFIER	c.*3077G>A\|	S112
83361	BAA01g44250	A01	29313333	G	A	missense_variant	MODERATE	c.1387G>A\|p.Asp463Asn	S293
83362	BAA01g44250	A01	29313376	C	T	missense_variant	MODERATE	c.1430C>T\|p.Ser477Phe	S221
83363	BAA01g44250	A01	29313575	G	A	missense_variant	MODERATE	c.1535G>A\|p.Ser512Asn	S86
83364	BAA01g44250	A01	29314835	C	T	synonymous_variant	LOW	c.2169C>T\|p.Asp723Asp	S25
83365	BAA01g44250	A01	29314893	C	T	missense_variant	MODERATE	c.2227C>T\|p.Leu743Phe	S188
83366	BAA01g44250	A01	29314994	G	A	synonymous_variant	LOW	c.2328G>A\|p.Val776Val	S117
83367	BAA01g44250	A01	29315247	G	A	missense_variant	MODERATE	c.2581G>A\|p.Glu861Lys	S225
83368	BAA01g44250	A01	29315339	C	T	downstream_gene_variant	MODIFIER	c.*69C>T\|	S88
83369	BAA01g44250	A01	29315824	A	C	downstream_gene_variant	MODIFIER	c.*554A>C\|	S176
83370	BAA01g44250	A01	29316183	G	A	downstream_gene_variant	MODIFIER	c.*913G>A\|	S108
83371	BAA01g44260	A01	29316425	C	T	missense_variant	MODERATE	c.1018G>A\|p.Asp340Asn	S94
83372	BAA01g44260	A01	29318663	G	A	upstream_gene_variant	MODIFIER	c.-432C>T\|	S121 S77
83373	BAA01g44260	A01	29318874	G	A	upstream_gene_variant	MODIFIER	c.-643C>T\|	S152
83374	BAA01g44260	A01	29322693	C	T	upstream_gene_variant	MODIFIER	c.-4462G>A\|	S134 S152 S155 S163 S166 S168 S171 S19 S213 S280 S67
83375	BAA01g44260	A01	29322907	G	A	upstream_gene_variant	MODIFIER	c.-4676C>T\|	S129

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