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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g26790	A01	15070956	C	T	upstream_gene_variant	MODIFIER	c.-4874C>T\|	S192
2	BAA01g26790	A01	15072208	G	A	upstream_gene_variant	MODIFIER	c.-3622G>A\|	S123
3	BAA01g26790	A01	15072225	C	T	upstream_gene_variant	MODIFIER	c.-3605C>T\|	S132 S137 S215
4	BAA01g26790	A01	15076829	C	T	synonymous_variant	LOW	c.612C>T\|p.Phe204Phe	S203
5	BAA01g26790	A01	15076852	G	A	missense_variant	MODERATE	c.635G>A\|p.Gly212Glu	S149
6	BAA01g26790	A01	15076981	C	T	missense_variant	MODERATE	c.764C>T\|p.Ser255Phe	S54
7	BAA01g26790	A01	15077261	G	A	downstream_gene_variant	MODIFIER	c.*246G>A\|	S159 S243 S276 S298 S299
8	BAA01g26790	A01	15078018	G	A	downstream_gene_variant	MODIFIER	c.*1003G>A\|	S105 S229
9	BAA01g26790	A01	15078035	C	T	downstream_gene_variant	MODIFIER	c.*1020C>T\|	S218
10	BAA01g26790	A01	15078293	G	A	downstream_gene_variant	MODIFIER	c.*1278G>A\|	S15 S2 S3 S34 S4 S6
11	BAA01g26790	A01	15078493	G	A	downstream_gene_variant	MODIFIER	c.*1478G>A\|	S181
12	BAA01g26790	A01	15078843	G	A	downstream_gene_variant	MODIFIER	c.*1828G>A\|	S98
13	BAA01g26790	A01	15079742	G	A	downstream_gene_variant	MODIFIER	c.*2727G>A\|	S178
14	BAA01g26790	A01	15080040	C	T	downstream_gene_variant	MODIFIER	c.*3025C>T\|	S20
15	BAA01g26790	A01	15080383	C	T	downstream_gene_variant	MODIFIER	c.*3368C>T\|	S186
16	BAA01g26790	A01	15080625	G	A	downstream_gene_variant	MODIFIER	c.*3610G>A\|	S236
17	BAA01g26790	A01	15081182	C	T	downstream_gene_variant	MODIFIER	c.*4167C>T\|	S112
18	BAA01g26790	A01	15081574	C	T	downstream_gene_variant	MODIFIER	c.*4559C>T\|	S249