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Search Results:

17 variations found. LOC_Os10g40830 (metalloendoproteinase 1 precursor; putative; expressed), ranging from 21,955,039 bp to 21,957,289 bp (including 0 kb upstream and 0 kb downstream of the gene).

Variation Map (with Chromatin Accessibility Map/ Non-coding Varation Scores Map) in Searched Region:

The 'big effect' variations are marked out:

ColorExplainDetails
red High impact variants defined by snpEff 'STOP_LOST', 'START_LOST', 'STOP_GAINED', 'FRAME_SHIFT' et. al., the details can be found at http://snpef f.sourceforge.net/SnpEff_manual.html#eff.
purple 'Damaging' or 'probably damaging' non-synonymous SNPs defined by PolyPhen-2 This is a qualitative result of nonsynonymous SNP annotation, where 'damaging' or 'probably damaging' means that the variant is more likely to affect protein function. Details can be found here.

Detailed Variation Information:

Var ID Chrom Position Primary Allele Secondary Allele Primary Allele Frequency DEL Frequency Var GWAS Results Effect
vg1021955049 (J) chr10 21955049 A G 63.40% 0.61% A -> G
mr1794 (Ind_All); LR P-value: 8.62E-08;
mr1860 (All); LR P-value: 2.40E-09;
mr1904 (Ind_All); LR P-value: 3.95E-06;
mr1183_2 (Ind_All); LR P-value: 1.39E-07;
mr1321_2 (All); LR P-value: 8.44E-07;
mr1322_2 (Ind_All); LR P-value: 9.24E-07;
mr1323_2 (Ind_All); LR P-value: 2.84E-06;
mr1330_2 (Ind_All); LR P-value: 3.73E-11;
mr1332_2 (All); LR P-value: 6.54E-06;
mr1336_2 (Ind_All); LR P-value: 2.27E-07;
mr1349_2 (All); LR P-value: 4.29E-11;
mr1360_2 (Ind_All); LR P-value: 7.50E-06;
mr1438_2 (Ind_All); LR P-value: 7.90E-06;
mr1478_2 (All); LR P-value: 8.43E-09;
mr1527_2 (Ind_All); LR P-value: 4.95E-07;
mr1540_2 (Ind_All); LR P-value: 2.68E-06;
mr1598_2 (All); LR P-value: 8.11E-36;
mr1598_2 (Ind_All); LR P-value: 7.89E-10;
mr1715_2 (Ind_All); LR P-value: 6.04E-12;
mr1728_2 (All); LR P-value: 2.91E-11;
mr1732_2 (Ind_All); LR P-value: 1.04E-06;
mr1754_2 (All); LR P-value: 1.00E-06;
mr1860_2 (All); LR P-value: 2.20E-09;
mr1875_2 (All); LR P-value: 5.06E-06;
mr1895_2 (All); LR P-value: 1.66E-07;
mr1895_2 (Ind_All); LR P-value: 8.25E-07;
mr1899_2 (All); LR P-value: 7.36E-06;
mr1910_2 (All); LR P-value: 5.20E-06;
mr1946_2 (All); LR P-value: 1.79E-10;
mr1948_2 (All); LR P-value: 1.79E-10;
mr1962_2 (Ind_All); LR P-value: 1.16E-08
LOC_Os10g40824.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40830.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955122 (J) chr10 21955122 C T 70.20% 0.47% C -> T
mr1090_2 (Ind_All); LR P-value: 6.33E-07;
mr1322_2 (Ind_All); LR P-value: 3.72E-06
LOC_Os10g40824.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40830.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955133 (J) chr10 21955133 A G 99.90% 0.00% A -> G NA
LOC_Os10g40824.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os10g40830.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os10g40820.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g40840.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955454 (J) chr10 21955454 C T 63.30% 0.61% C -> T
mr1717 (All); LR P-value: 1.24E-07;
mr1794 (Ind_All); LR P-value: 2.51E-08;
mr1860 (All); LR P-value: 1.19E-08;
mr1183_2 (Ind_All); LR P-value: 1.13E-07;
mr1321_2 (All); LR P-value: 2.63E-07;
mr1322_2 (Ind_All); LR P-value: 8.45E-07;
mr1323_2 (Ind_All); LR P-value: 1.57E-06;
mr1330_2 (Ind_All); LR P-value: 5.53E-11;
mr1336_2 (Ind_All); LR P-value: 2.74E-07;
mr1349_2 (All); LR P-value: 1.74E-11;
mr1355_2 (All); LR P-value: 4.50E-06;
mr1360_2 (Ind_All); LR P-value: 9.98E-06;
mr1438_2 (Ind_All); LR P-value: 5.37E-06;
mr1479_2 (All); LR P-value: 1.44E-06;
mr1527_2 (Ind_All); LR P-value: 1.13E-06;
mr1540_2 (Ind_All); LR P-value: 2.14E-06;
mr1598_2 (All); LR P-value: 2.12E-32;
mr1598_2 (Ind_All); LR P-value: 1.02E-09;
mr1715_2 (Ind_All); LR P-value: 4.69E-12;
mr1717_2 (All); LR P-value: 9.06E-13;
mr1728_2 (All); LR P-value: 2.89E-11;
mr1732_2 (Ind_All); LR P-value: 8.62E-07;
mr1754_2 (All); LR P-value: 1.58E-06;
mr1860_2 (All); LR P-value: 3.71E-10;
mr1895_2 (All); LR P-value: 4.24E-07;
mr1895_2 (Ind_All); LR P-value: 6.73E-07;
mr1904_2 (Ind_All); LR P-value: 1.09E-06;
mr1910_2 (All); LR P-value: 4.50E-06;
mr1946_2 (All); LR P-value: 3.20E-09;
mr1948_2 (All); LR P-value: 3.20E-09
LOC_Os10g40824.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40830.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955624 (J) chr10 21955624 CT CTT 98.20% 0.00% CT -> CTT,C NA
LOC_Os10g40830.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40830.1 Alt: CTT| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: CTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: CTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: CTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955625 (J) chr10 21955625 T A 98.20% 1.14% T -> A NA
LOC_Os10g40830.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955677 (J) chr10 21955677 T C 63.50% 0.11% T -> C
Grain_width (Ind_All); LR P-value: 2.87E-10;
mr1503 (Ind_All); LR P-value: 1.13E-06;
mr1717 (All); LR P-value: 2.01E-07;
mr1794 (Ind_All); LR P-value: 8.82E-08;
mr1860 (All); LR P-value: 3.53E-09;
mr1183_2 (Ind_All); LR P-value: 7.42E-08;
mr1321_2 (All); LR P-value: 3.39E-07;
mr1322_2 (Ind_All); LR P-value: 4.79E-07;
mr1323_2 (Ind_All); LR P-value: 1.00E-06;
mr1330_2 (Ind_All); LR P-value: 2.80E-11;
mr1332_2 (All); LR P-value: 6.61E-06;
mr1336_2 (Ind_All); LR P-value: 1.27E-07;
mr1349_2 (All); LR P-value: 1.58E-11;
mr1349_2 (Ind_All); LR P-value: 5.61E-06;
mr1355_2 (All); LR P-value: 5.83E-06;
mr1360_2 (Ind_All); LR P-value: 2.95E-06;
mr1478_2 (All); LR P-value: 6.06E-09;
mr1527_2 (Ind_All); LR P-value: 1.39E-06;
mr1540_2 (Ind_All); LR P-value: 1.30E-06;
mr1598_2 (All); LR P-value: 1.19E-34;
mr1598_2 (Ind_All); LR P-value: 4.97E-09;
mr1715_2 (Ind_All); LR P-value: 9.85E-13;
mr1728_2 (All); LR P-value: 2.72E-11;
mr1732_2 (Ind_All); LR P-value: 3.93E-07;
mr1754_2 (All); LR P-value: 3.09E-06;
mr1860_2 (All); LR P-value: 1.15E-09;
mr1895_2 (All); LR P-value: 8.52E-08;
mr1895_2 (Ind_All); LR P-value: 3.27E-07;
mr1899_2 (All); LR P-value: 6.89E-06;
mr1910_2 (All); LR P-value: 3.76E-06;
mr1946_2 (All); LR P-value: 3.18E-10;
mr1948_2 (All); LR P-value: 3.18E-10
LOC_Os10g40830.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955737 (J) chr10 21955737 C G 70.20% 0.59% C -> G
mr1717 (All); LR P-value: 5.92E-07;
mr1090_2 (Ind_All); LR P-value: 2.71E-07;
mr1322_2 (Ind_All); LR P-value: 4.27E-06;
mr1679_2 (Ind_All); LR P-value: 8.20E-06
LOC_Os10g40830.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os10g40830.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021955776 (J) chr10 21955776 T A 63.50% 0.51% T -> A
Grain_length (Ind_All); LR P-value: 2.01E-13;
mr1441 (Ind_All); LR P-value: 2.14E-06;
mr1503 (Ind_All); LR P-value: 6.45E-07;
mr1715 (Ind_All); LR P-value: 2.67E-06;
mr1717 (All); LR P-value: 9.02E-08;
mr1794 (Ind_All); LR P-value: 1.22E-08;
mr1860 (All); LR P-value: 6.16E-09;
mr1183_2 (Ind_All); LR P-value: 5.45E-08;
mr1319_2 (Ind_All); LR P-value: 4.73E-06;
mr1321_2 (All); LR P-value: 7.34E-07;
mr1322_2 (Ind_All); LR P-value: 5.35E-07;
mr1323_2 (Ind_All); LR P-value: 1.43E-06;
mr1330_2 (Ind_All); LR P-value: 4.82E-11;
mr1332_2 (All); LR P-value: 5.51E-06;
mr1336_2 (Ind_All); LR P-value: 3.62E-07;
mr1349_2 (All); LR P-value: 2.97E-11;
mr1360_2 (Ind_All); LR P-value: 9.90E-06;
mr1438_2 (Ind_All); LR P-value: 3.50E-06;
mr1527_2 (Ind_All); LR P-value: 1.45E-06;
mr1540_2 (Ind_All); LR P-value: 1.99E-06;
mr1598_2 (All); LR P-value: 1.66E-36;
mr1598_2 (Ind_All); LR P-value: 3.05E-10;
mr1715_2 (Ind_All); LR P-value: 5.51E-12;
mr1728_2 (All); LR P-value: 4.83E-11;
mr1732_2 (Ind_All); LR P-value: 1.00E-06;
mr1754_2 (All); LR P-value: 9.16E-07;
mr1860_2 (All); LR P-value: 6.33E-09;
mr1875_2 (All); LR P-value: 4.54E-06;
mr1895_2 (All); LR P-value: 7.55E-08;
mr1895_2 (Ind_All); LR P-value: 6.34E-07;
mr1910_2 (All); LR P-value: 2.92E-06;
mr1946_2 (All); LR P-value: 2.70E-09;
mr1948_2 (All); LR P-value: 2.70E-09
LOC_Os10g40830.1 Alt: A| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
LOC_Os10g40830.1 Alt: DEL/frameshift_variant(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021956177 (J) chr10 21956177 G A 98.90% 0.00% G -> A NA
LOC_Os10g40830.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021956657 (J) chr10 21956657 G GCCGTGC CCGTGC 63.50% 0.00% G -> GCCGTGCCCG TGC NA
LOC_Os10g40830.1 Alt: GCCGTGCCCGTGC| disruptive_inframe_insertion MODERATE(snpEff)/inframe_variant(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021956826 (J) chr10 21956826 C T 63.50% 0.40% C -> T
mr1717 (All); LR P-value: 1.86E-07;
mr1794 (Ind_All); LR P-value: 2.51E-08;
mr1860 (All); LR P-value: 1.12E-08;
mr1183_2 (Ind_All); LR P-value: 1.13E-07;
mr1321_2 (All); LR P-value: 6.06E-07;
mr1322_2 (Ind_All); LR P-value: 8.45E-07;
mr1323_2 (Ind_All); LR P-value: 1.57E-06;
mr1330_2 (Ind_All); LR P-value: 5.53E-11;
mr1336_2 (Ind_All); LR P-value: 2.74E-07;
mr1349_2 (All); LR P-value: 3.53E-11;
mr1355_2 (All); LR P-value: 9.83E-06;
mr1360_2 (Ind_All); LR P-value: 9.98E-06;
mr1438_2 (Ind_All); LR P-value: 5.37E-06;
mr1478_2 (All); LR P-value: 1.07E-08;
mr1527_2 (Ind_All); LR P-value: 1.13E-06;
mr1540_2 (Ind_All); LR P-value: 2.14E-06;
mr1598_2 (All); LR P-value: 6.99E-36;
mr1598_2 (Ind_All); LR P-value: 1.02E-09;
mr1715_2 (Ind_All); LR P-value: 4.69E-12;
mr1728_2 (All); LR P-value: 2.81E-11;
mr1732_2 (Ind_All); LR P-value: 8.62E-07;
mr1754_2 (All); LR P-value: 4.61E-07;
mr1860_2 (All); LR P-value: 2.88E-09;
mr1895_2 (All); LR P-value: 1.51E-07;
mr1895_2 (Ind_All); LR P-value: 6.73E-07;
mr1904_2 (Ind_All); LR P-value: 1.09E-06;
mr1910_2 (All); LR P-value: 3.46E-06;
mr1946_2 (All); LR P-value: 6.56E-10;
mr1948_2 (All); LR P-value: 6.56E-10
LOC_Os10g40830.1 Alt: T| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021957010 (J) chr10 21957010 T G 63.30% 0.47% T -> G
Grain_width (Ind_All); LR P-value: 2.49E-10;
mr1503 (Ind_All); LR P-value: 8.87E-07;
mr1717 (All); LR P-value: 2.17E-07;
mr1794 (Ind_All); LR P-value: 1.69E-08;
mr1860 (All); LR P-value: 6.14E-09;
mr1183_2 (Ind_All); LR P-value: 6.18E-08;
mr1321_2 (All); LR P-value: 2.19E-07;
mr1322_2 (Ind_All); LR P-value: 5.60E-07;
mr1323_2 (Ind_All); LR P-value: 1.20E-06;
mr1330_2 (Ind_All); LR P-value: 1.38E-11;
mr1332_2 (All); LR P-value: 9.97E-06;
mr1336_2 (Ind_All); LR P-value: 1.65E-07;
mr1349_2 (All); LR P-value: 1.13E-11;
mr1349_2 (Ind_All); LR P-value: 6.05E-06;
mr1355_2 (All); LR P-value: 3.70E-06;
mr1360_2 (Ind_All); LR P-value: 4.14E-06;
mr1438_2 (Ind_All); LR P-value: 4.78E-06;
mr1478_2 (All); LR P-value: 1.75E-08;
mr1479_2 (All); LR P-value: 1.54E-06;
mr1527_2 (Ind_All); LR P-value: 4.80E-07;
mr1540_2 (Ind_All); LR P-value: 1.07E-06;
mr1598_2 (All); LR P-value: 1.33E-31;
mr1598_2 (Ind_All); LR P-value: 2.13E-09;
mr1715_2 (Ind_All); LR P-value: 2.38E-12;
mr1717_2 (All); LR P-value: 9.89E-13;
mr1728_2 (All); LR P-value: 4.53E-11;
mr1732_2 (Ind_All); LR P-value: 4.36E-07;
mr1754_2 (All); LR P-value: 2.31E-06;
mr1860_2 (All); LR P-value: 3.22E-10;
mr1895_2 (All); LR P-value: 3.58E-07;
mr1895_2 (Ind_All); LR P-value: 4.13E-07;
mr1899_2 (All); LR P-value: 7.32E-06;
mr1910_2 (All); LR P-value: 4.60E-06;
mr1946_2 (All); LR P-value: 1.69E-09;
mr1948_2 (All); LR P-value: 1.69E-09
LOC_Os10g40830.1 Alt: G| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021957237 (J) chr10 21957237 G T 93.40% 0.00% G -> T
mr1692 (Ind_All); LR P-value: 7.35E-06;
mr1045_2 (All); LR P-value: 5.42E-07;
mr1045_2 (Ind_All); LR P-value: 6.86E-06;
mr1053_2 (All); LR P-value: 6.75E-07;
mr1115_2 (Ind_All); LR P-value: 3.91E-07;
mr1236_2 (Ind_All); LR P-value: 6.25E-07;
mr1306_2 (Ind_All); LR P-value: 7.89E-06;
mr1517_2 (Ind_All); LR P-value: 1.16E-06;
mr1611_2 (Ind_All); LR P-value: 6.93E-07;
mr1641_2 (Ind_All); LR P-value: 1.78E-06;
mr1696_2 (Ind_All); LR P-value: 8.31E-07;
mr1735_2 (Ind_All); LR P-value: 4.99E-06;
mr1758_2 (Ind_All); LR P-value: 2.17E-08;
mr1763_2 (All); LR P-value: 2.17E-06;
mr1820_2 (Ind_All); LR P-value: 9.35E-06;
mr1838_2 (Ind_All); LR P-value: 8.15E-08;
mr1876_2 (All); LR P-value: 3.60E-06;
mr1901_2 (All); LR P-value: 2.05E-06;
mr1906_2 (Ind_All); LR P-value: 5.91E-06;
mr1909_2 (Ind_All); LR P-value: 3.00E-06;
mr1959_2 (Ind_All); LR P-value: 4.50E-07;
mr1960_2 (Ind_All); LR P-value: 4.79E-06
LOC_Os10g40830.1 Alt: T| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: T| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021957258 (J) chr10 21957258 G A 63.20% 0.47% G -> A
Grain_width (Ind_All); LR P-value: 2.49E-10;
mr1503 (Ind_All); LR P-value: 8.87E-07;
mr1717 (All); LR P-value: 2.14E-07;
mr1794 (Ind_All); LR P-value: 1.69E-08;
mr1860 (All); LR P-value: 4.80E-09;
mr1183_2 (Ind_All); LR P-value: 6.18E-08;
mr1321_2 (All); LR P-value: 2.15E-07;
mr1322_2 (Ind_All); LR P-value: 5.60E-07;
mr1323_2 (Ind_All); LR P-value: 1.20E-06;
mr1330_2 (Ind_All); LR P-value: 1.38E-11;
mr1332_2 (All); LR P-value: 6.64E-06;
mr1336_2 (Ind_All); LR P-value: 1.65E-07;
mr1349_2 (All); LR P-value: 5.36E-12;
mr1349_2 (Ind_All); LR P-value: 6.05E-06;
mr1355_2 (All); LR P-value: 2.85E-06;
mr1360_2 (Ind_All); LR P-value: 4.14E-06;
mr1438_2 (Ind_All); LR P-value: 4.78E-06;
mr1462_2 (All); LR P-value: 7.71E-06;
mr1479_2 (All); LR P-value: 1.79E-06;
mr1527_2 (Ind_All); LR P-value: 4.80E-07;
mr1540_2 (Ind_All); LR P-value: 1.07E-06;
mr1598_2 (All); LR P-value: 9.62E-32;
mr1598_2 (Ind_All); LR P-value: 2.13E-09;
mr1715_2 (Ind_All); LR P-value: 2.38E-12;
mr1717_2 (All); LR P-value: 5.29E-13;
mr1728_2 (All); LR P-value: 2.37E-11;
mr1732_2 (Ind_All); LR P-value: 4.36E-07;
mr1754_2 (All); LR P-value: 2.02E-06;
mr1860_2 (All); LR P-value: 2.56E-10;
mr1895_2 (All); LR P-value: 2.08E-07;
mr1895_2 (Ind_All); LR P-value: 4.13E-07;
mr1899_2 (All); LR P-value: 7.47E-06;
mr1910_2 (All); LR P-value: 3.51E-06;
mr1946_2 (All); LR P-value: 2.45E-09;
mr1948_2 (All); LR P-value: 2.45E-09
LOC_Os10g40830.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40820.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40840.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os10g40824.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
vg1021957284 (J) chr10 21957284 G A 99.40% 0.00% G -> A NA
LOC_Os10g40830.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)
LOC_Os10g40820.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g40840.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os10g40824.1 Alt: A| downstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 4.210; most accessible tissue: Minghui63 panicle, score: 7.125
STR1021956658 (J) chr10 21956658 CCGTGCC CGTGC CCGTGCC CGTGCCC GTGCCCG TGC 68.10% 0.00% CCGTGCCCGT GC -> CCGTGCCCGT GCCCGTGCCC GTGC NA