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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g19410	A10	17797479	C	T	upstream_gene_variant	MODIFIER	c.-4816C>T\|	S152
2	BAA10g19410	A10	17797565	C	T	upstream_gene_variant	MODIFIER	c.-4730C>T\|	S177
3	BAA10g19410	A10	17797580	C	T	upstream_gene_variant	MODIFIER	c.-4715C>T\|	S60
4	BAA10g19410	A10	17797610	G	A	upstream_gene_variant	MODIFIER	c.-4685G>A\|	S172 S217
5	BAA10g19410	A10	17800179	C	T	upstream_gene_variant	MODIFIER	c.-2116C>T\|	S299
6	BAA10g19410	A10	17800853	C	A	upstream_gene_variant	MODIFIER	c.-1442C>A\|	S112 S12 S130 S131 S137 S164 S174 S185 S209 S215 S232 S244 S259 S262 S286 S301 S302 S78 S85
7	BAA10g19410	A10	17801326	C	T	upstream_gene_variant	MODIFIER	c.-969C>T\|	S61
8	BAA10g19410	A10	17801384	G	A	upstream_gene_variant	MODIFIER	c.-911G>A\|	S28
9	BAA10g19410	A10	17801414	C	T	upstream_gene_variant	MODIFIER	c.-881C>T\|	S251
10	BAA10g19410	A10	17802496	C	T	synonymous_variant	LOW	c.202C>T\|p.Leu68Leu	S301 S304
11	BAA10g19410	A10	17802615	C	T	synonymous_variant	LOW	c.321C>T\|p.Asn107Asn	S76
12	BAA10g19410	A10	17802881	G	A	missense_variant	MODERATE	c.418G>A\|p.Gly140Ser	S164
13	BAA10g19410	A10	17803480	C	T	splice_region_variant&synonymous_variant	LOW	c.789C>T\|p.Ser263Ser	S282