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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
64551	BAA01g33850	A01	22619903	C	T	upstream_gene_variant	MODIFIER	c.-4225G>A\|	S85
64552	BAA01g33850	A01	22620114	G	A	upstream_gene_variant	MODIFIER	c.-4436C>T\|	S87
64553	BAA01g33850-BAA01g33860	A01	22620839	G	A	intergenic_region	MODIFIER	n.22620839G>A\|	S299
64554	BAA01g33850-BAA01g33860	A01	22620985	C	T	intergenic_region	MODIFIER	n.22620985C>T\|	S132 S137 S215
64555	BAA01g33850-BAA01g33860	A01	22621102	C	T	intergenic_region	MODIFIER	n.22621102C>T\|	S104 S52
64556	BAA01g33850-BAA01g33860	A01	22621821	C	T	intergenic_region	MODIFIER	n.22621821C>T\|	S303
64557	BAA01g33850-BAA01g33860	A01	22621854	C	T	intergenic_region	MODIFIER	n.22621854C>T\|	S153
64558	BAA01g33850-BAA01g33860	A01	22621864	T	G	intergenic_region	MODIFIER	n.22621864T>G\|	S208 S93
64559	BAA01g33850-BAA01g33860	A01	22621971	C	T	intergenic_region	MODIFIER	n.22621971C>T\|	S180 S250
64560	BAA01g33860	A01	22623572	G	A	downstream_gene_variant	MODIFIER	c.*3989C>T\|	S119 S274
64561	BAA01g33860	A01	22624278	C	T	downstream_gene_variant	MODIFIER	c.*3283G>A\|	S107
64562	BAA01g33860	A01	22624330	G	A	downstream_gene_variant	MODIFIER	c.*3231C>T\|	S199
64563	BAA01g33860	A01	22624522	A	T	downstream_gene_variant	MODIFIER	c.*3039T>A\|	S99
64564	BAA01g33860	A01	22626007	C	T	downstream_gene_variant	MODIFIER	c.*1554G>A\|	S50
64565	BAA01g33860	A01	22627043	C	T	downstream_gene_variant	MODIFIER	c.*518G>A\|	S142
64566	BAA01g33860	A01	22627173	C	T	downstream_gene_variant	MODIFIER	c.*388G>A\|	S44
64567	BAA01g33860	A01	22627446	G	A	downstream_gene_variant	MODIFIER	c.*115C>T\|	S278
64568	BAA01g33860	A01	22627755	C	T	missense_variant&splice_region_variant	MODERATE	c.1414G>A\|p.Val472Met	S213
64569	BAA01g33860	A01	22628092	C	T	missense_variant	MODERATE	c.1306G>A\|p.Val436Ile	S193
64570	BAA01g33860	A01	22628131	C	T	missense_variant	MODERATE	c.1267G>A\|p.Glu423Lys	S150
64571	BAA01g33860	A01	22628340	C	T	missense_variant	MODERATE	c.1058G>A\|p.Arg353Lys	S19
64572	BAA01g33860	A01	22628744	C	T	synonymous_variant	LOW	c.654G>A\|p.Leu218Leu	S57
64573	BAA01g33860	A01	22628905	C	T	missense_variant	MODERATE	c.493G>A\|p.Asp165Asn	S64
64574	BAA01g33860	A01	22628961	G	A	missense_variant	MODERATE	c.437C>T\|p.Ala146Val	S292
64575	BAA01g33860	A01	22630243	C	T	upstream_gene_variant	MODIFIER	c.-846G>A\|	S120

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