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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
69201	BAA01g36200	A01	24264797	G	A	downstream_gene_variant	MODIFIER	c.*1796G>A\|	S157 S163
69202	BAA01g36200	A01	24264865	G	A	downstream_gene_variant	MODIFIER	c.*1864G>A\|	S196
69203	BAA01g36200	A01	24265026	G	A	downstream_gene_variant	MODIFIER	c.*2025G>A\|	S259
69204	BAA01g36210	A01	24266624	G	A	upstream_gene_variant	MODIFIER	c.-4522G>A\|	S149
69205	BAA01g36210	A01	24267430	C	T	upstream_gene_variant	MODIFIER	c.-3716C>T\|	S210 S225
69206	BAA01g36210	A01	24268537	G	A	upstream_gene_variant	MODIFIER	c.-2609G>A\|	S1 S90
69207	BAA01g36210	A01	24269941	C	T	upstream_gene_variant	MODIFIER	c.-1205C>T\|	S219 S72
69208	BAA01g36210	A01	24270734	G	T	upstream_gene_variant	MODIFIER	c.-412G>T\|	S170
69209	BAA01g36220	A01	24271276	G	A	upstream_gene_variant	MODIFIER	c.-4120G>A\|	S67
69210	BAA01g36210	A01	24271336	C	T	stop_gained	HIGH	c.103C>T\|p.Arg35*	S192
69211	BAA01g36210	A01	24271767	G	A	missense_variant	MODERATE	c.331G>A\|p.Asp111Asn	S296
69212	BAA01g36210	A01	24272224	C	T	missense_variant	MODERATE	c.788C>T\|p.Pro263Leu	S255
69213	BAA01g36210	A01	24272282	A	G	synonymous_variant	LOW	c.846A>G\|p.Leu282Leu	S198
69214	BAA01g36220	A01	24272493	C	T	upstream_gene_variant	MODIFIER	c.-2903C>T\|	S107
69215	BAA01g36220	A01	24272619	C	A	upstream_gene_variant	MODIFIER	c.-2777C>A\|	S275
69216	BAA01g36210	A01	24273085	C	T	missense_variant	MODERATE	c.1154C>T\|p.Pro385Leu	S186
69217	BAA01g36210	A01	24273133	G	A	missense_variant	MODERATE	c.1202G>A\|p.Arg401Gln	S33
69218	BAA01g36220	A01	24275269	C	T	upstream_gene_variant	MODIFIER	c.-127C>T\|	S183 S198
69219	BAA01g36210	A01	24276169	G	A	downstream_gene_variant	MODIFIER	c.*1853G>A\|	S25
69220	BAA01g36230	A01	24277110	G	A	upstream_gene_variant	MODIFIER	c.-4126G>A\|	S292
69221	BAA01g36230	A01	24277514	G	A	upstream_gene_variant	MODIFIER	c.-3722G>A\|	S217 S248
69222	BAA01g36230	A01	24280982	C	T	upstream_gene_variant	MODIFIER	c.-254C>T\|	S11
69223	BAA01g36230	A01	24281793	C	T	synonymous_variant	LOW	c.558C>T\|p.Leu186Leu	S183 S198
69224	BAA01g36230	A01	24281810	C	T	missense_variant	MODERATE	c.575C>T\|p.Ser192Phe	S128
69225	BAA01g36240	A01	24283087	C	T	upstream_gene_variant	MODIFIER	c.-501C>T\|	S240

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