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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g10850	A10	12596932	G	A	upstream_gene_variant	MODIFIER	c.-1660G>A\|	S39
2	BAA10g10850	A10	12597013	C	T	upstream_gene_variant	MODIFIER	c.-1579C>T\|	S98
3	BAA10g10850	A10	12598481	G	A	upstream_gene_variant	MODIFIER	c.-111G>A\|	S255
4	BAA10g10850	A10	12598486	G	A	upstream_gene_variant	MODIFIER	c.-106G>A\|	S240
5	BAA10g10850	A10	12598995	G	A	missense_variant	MODERATE	c.143G>A\|p.Gly48Glu	S67
6	BAA10g10850	A10	12599400	G	A	synonymous_variant	LOW	c.270G>A\|p.Arg90Arg	S11
7	BAA10g10850	A10	12600240	T	C	downstream_gene_variant	MODIFIER	c.*560T>C\|	S278
8	BAA10g10850	A10	12601011	C	T	downstream_gene_variant	MODIFIER	c.*1331C>T\|	S175 S177
9	BAA10g10850	A10	12601594	G	A	downstream_gene_variant	MODIFIER	c.*1914G>A\|	S293
10	BAA10g10850	A10	12601965	C	T	downstream_gene_variant	MODIFIER	c.*2285C>T\|	S246
11	BAA10g10850	A10	12603923	C	T	downstream_gene_variant	MODIFIER	c.*4243C>T\|	S297
12	BAA10g10850	A10	12604050	G	A	downstream_gene_variant	MODIFIER	c.*4370G>A\|	S176
13	BAA10g10850	A10	12604514	A	T	downstream_gene_variant	MODIFIER	c.*4834A>T\|	S11 S130 S155 S210 S212 S213 S260
14	BAA10g10850	A10	12604534	A	C	downstream_gene_variant	MODIFIER	c.*4854A>C\|	S124 S210 S213 S227 S237 S278 S85
15	BAA10g10850	A10	12604543	C	T	downstream_gene_variant	MODIFIER	c.*4863C>T\|	S116