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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
100551	BAA10g06980-BAA10g06990	A10	3764473	C	T	intergenic_region	MODIFIER	n.3764473C>T\|	S193
100552	BAA10g06980-BAA10g06990	A10	3765102	C	T	intergenic_region	MODIFIER	n.3765102C>T\|	S42
100553	BAA10g06980-BAA10g06990	A10	3765608	C	T	intergenic_region	MODIFIER	n.3765608C>T\|	S206 S26
100554	BAA10g06980-BAA10g06990	A10	3765641	C	T	intergenic_region	MODIFIER	n.3765641C>T\|	S152
100555	BAA10g06980-BAA10g06990	A10	3765805	G	A	intergenic_region	MODIFIER	n.3765805G>A\|	S51
100556	BAA10g06980-BAA10g06990	A10	3766684	C	T	intergenic_region	MODIFIER	n.3766684C>T\|	S282
100557	BAA10g06980-BAA10g06990	A10	3766766	G	A	intergenic_region	MODIFIER	n.3766766G>A\|	S129
100558	BAA10g06980-BAA10g06990	A10	3766822	G	A	intergenic_region	MODIFIER	n.3766822G>A\|	S148 S30 S31
100559	BAA10g06980-BAA10g06990	A10	3767270	C	T	intergenic_region	MODIFIER	n.3767270C>T\|	S187
100560	BAA10g06980-BAA10g06990	A10	3767381	G	A	intergenic_region	MODIFIER	n.3767381G>A\|	S164
100561	BAA10g06980-BAA10g06990	A10	3767651	G	A	intergenic_region	MODIFIER	n.3767651G>A\|	S3
100562	BAA10g06980-BAA10g06990	A10	3768697	G	A	intergenic_region	MODIFIER	n.3768697G>A\|	S111
100563	BAA10g06980-BAA10g06990	A10	3769157	G	A	intergenic_region	MODIFIER	n.3769157G>A\|	S234
100564	BAA10g06980-BAA10g06990	A10	3769995	C	T	intergenic_region	MODIFIER	n.3769995C>T\|	S193
100565	BAA10g06980-BAA10g06990	A10	3770504	G	A	intergenic_region	MODIFIER	n.3770504G>A\|	S1 S90
100566	BAA10g06980-BAA10g06990	A10	3770995	G	A	intergenic_region	MODIFIER	n.3770995G>A\|	S95
100567	BAA10g06980-BAA10g06990	A10	3771996	C	A	intergenic_region	MODIFIER	n.3771996C>A\|	S197
100568	BAA10g06980-BAA10g06990	A10	3772879	G	A	intergenic_region	MODIFIER	n.3772879G>A\|	S125
100569	BAA10g06980-BAA10g06990	A10	3773379	C	T	intergenic_region	MODIFIER	n.3773379C>T\|	S110
100570	BAA10g06980-BAA10g06990	A10	3773722	C	T	intergenic_region	MODIFIER	n.3773722C>T\|	S239
100571	BAA10g06980-BAA10g06990	A10	3773992	G	A	intergenic_region	MODIFIER	n.3773992G>A\|	S303
100572	BAA10g06980-BAA10g06990	A10	3774338	C	T	intergenic_region	MODIFIER	n.3774338C>T\|	S71
100573	BAA10g06980-BAA10g06990	A10	3774391	G	A	intergenic_region	MODIFIER	n.3774391G>A\|	S174 S216 S241 S265 S27 S39
100574	BAA10g06980-BAA10g06990	A10	3774493	C	T	intergenic_region	MODIFIER	n.3774493C>T\|	S143
100575	BAA10g06980-BAA10g06990	A10	3774823	C	T	intergenic_region	MODIFIER	n.3774823C>T\|	S123

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