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Detailed information for vg1221857564:

Variant ID: vg1221857564 (JBrowse)	Variation Type: SNP
Chromosome: chr12	Position: 21857564
Reference Allele: C	Alternative Allele: T
Primary Allele: C	Secondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:

CGCCGTCACCACCGTGCCATCGCCGGAGCTGCTGCTGAGAGGGAGGAGTGGGGAGAGGAGTAGGGGAGTGGGGAGAGATAGAGCCAGGAGAGGAGAGGAT[C/T]
GAGTGGAGTGGGTGATGGAGAGAGAGAGGAGTTGAGATTAAAGAATGGAAGTGGGAATCTTTTCGGGTCTTTTTGCATGCGGATGAGTTAAGTGCCCCGC

Reverse complement sequence

GCGGGGCACTTAACTCATCCGCATGCAAAAAGACCCGAAAAGATTCCCACTTCCATTCTTTAATCTCAACTCCTCTCTCTCTCCATCACCCACTCCACTC[G/A]
ATCCTCTCCTCTCCTGGCTCTATCTCTCCCCACTCCCCTACTCCTCTCCCCACTCCTCCCTCTCAGCAGCAGCTCCGGCGATGGCACGGTGGTGACGGCG

Allele Frequencies:

Populations	Population Size	Frequency of C(primary allele)	Frequency of T(secondary allele)	Frequency of N	Frequency of DEL	Frequency of others Allele
All	4726	44.80%	8.70%	0.80%	45.64%	NA
All Indica	2759	29.20%	4.10%	1.16%	65.53%	NA
All Japonica	1512	77.30%	17.70%	0.26%	4.76%	NA
Aus	269	15.20%	1.10%	0.74%	82.90%	NA
Indica I	595	4.20%	12.90%	1.01%	81.85%	NA
Indica II	465	77.60%	0.20%	0.65%	21.51%	NA
Indica III	913	19.60%	1.90%	0.88%	77.66%	NA
Indica Intermediate	786	30.70%	2.30%	1.91%	65.14%	NA
Temperate Japonica	767	93.90%	2.30%	0.52%	3.26%	NA
Tropical Japonica	504	59.70%	32.10%	0.00%	8.13%	NA
Japonica Intermediate	241	61.40%	36.10%	0.00%	2.49%	NA
VI/Aromatic	96	38.50%	24.00%	0.00%	37.50%	NA
Intermediate	90	72.20%	7.80%	0.00%	20.00%	NA

Allele Effect:

Var ID	Var	Locus	snpEff Annotation	CooVar Annotation	Chromatin Accessibility Score	PolyPhen-2 Effect	PolyPhen-2 Score	SIFT Effect	SIFT Score
vg1221857564	C -> DEL	N	N	silent_mutation	Average:46.862; most accessible tissue: Minghui63 panicle, score: 89.444	N	N	N	N
vg1221857564	C -> T	LOC_Os12g35870.1	upstream_gene_variant ; 176.0bp to feature; MODIFIER	silent_mutation	Average:46.862; most accessible tissue: Minghui63 panicle, score: 89.444	N	N	N	N
vg1221857564	C -> T	LOC_Os12g35880.1	upstream_gene_variant ; 1684.0bp to feature; MODIFIER	silent_mutation	Average:46.862; most accessible tissue: Minghui63 panicle, score: 89.444	N	N	N	N
vg1221857564	C -> T	LOC_Os12g35860.1	downstream_gene_variant ; 4967.0bp to feature; MODIFIER	silent_mutation	Average:46.862; most accessible tissue: Minghui63 panicle, score: 89.444	N	N	N	N
vg1221857564	C -> T	LOC_Os12g35870-LOC_Os12g35880	intergenic_region ; MODIFIER	silent_mutation	Average:46.862; most accessible tissue: Minghui63 panicle, score: 89.444	N	N	N	N

Effects Predicted by Deep Convolutional Neural Networks

For each variant, we constructed two sequences that contain the variation site and the sequence around it, differing only in the variation site. We then used Basenji to predict the chromatin accessibility of each tissue for the two sequences, respectively, and scored the effect of the variant by comparing the changes in chromatin accessibility corresponding to the two genotypes in the 1 kb region around the variation site. The effect score was defined as the logarithmic ratio of the predicted chromatin accessibility of the alternative genotype to the value of the reference genotype.

Var ID	Ref	Alt	Root (RT)	Young Leaf (YL)	Flag Leaf (FL)	Young Panicle (YP)	Lemma & Palea (LP)	Stamen & Pistil (SP)
vg1221857564	C	T	0.0	0.01	0.0	0.01	0.0	0.0

Putative Genotype-Phenotype Associations:

Var ID	LMM P-value	LR P-value	Trait	Subpopulation	Is leadSNP	Publication
vg1221857564	5.52E-07	5.52E-07	mr1261	Jap_All	YES	Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251