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Search Results:

19 variations found. Os04g0494800/LOC_Os04g41740 (expressed protein), ranging from 24,740,702 bp to 24,742,677 bp (including 0 kb upstream and 0 kb downstream of the gene).

Gene IDAnnotation
LOC_Os04g41740 expressed protein; RAP ID: Os04g0494800; MSU ID: LOC_Os04g41740

Gene Expression Atlas:

The expression data is from the CREP database. And the expression value is log2-transformed. Move the mouse over the cells of the heat map to get detailed tissue information and expression values.

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
vg0424740725 (J) chr04 24740725 A G 59.80% 0.63% G -> A
mr1379 (All); LR P-value: 1.03E-09;
mr1509 (All); LR P-value: 5.15E-41;
mr1571 (All); LR P-value: 2.88E-24;
mr1580 (All); LR P-value: 4.02E-22;
mr1825 (All); LR P-value: 5.65E-19;
mr1335_2 (All); LR P-value: 1.24E-07;
mr1524_2 (All); LR P-value: 5.73E-06;
mr1559_2 (All); LR P-value: 1.86E-06;
mr1578_2 (All); LR P-value: 3.98E-15;
mr1579_2 (All); LR P-value: 2.30E-14;
mr1580_2 (All); LR P-value: 1.02E-30;
mr1666_2 (All); LR P-value: 9.07E-12;
mr1698_2 (All); LR P-value: 2.81E-21;
mr1825_2 (All); LR P-value: 1.64E-29;
mr1924_2 (All); LR P-value: 1.11E-20
N Alt: DEL/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 88.175; most accessible tissue: Minghui63 root, score: 96.290
vg0424741072 (J) chr04 24741072 C T 59.90% 0.66% T -> C
mr1379 (All); LR P-value: 1.38E-09;
mr1509 (All); LR P-value: 6.58E-42;
mr1571 (All); LR P-value: 7.02E-24;
mr1580 (All); LR P-value: 9.52E-22;
mr1731 (All); LR P-value: 1.20E-24;
mr1825 (All); LR P-value: 5.54E-19;
mr1524_2 (All); LR P-value: 5.87E-06;
mr1559_2 (All); LR P-value: 3.03E-06;
mr1578_2 (All); LR P-value: 2.97E-15;
mr1580_2 (All); LR P-value: 3.32E-30;
mr1666_2 (All); LR P-value: 4.41E-12;
mr1698_2 (All); LR P-value: 2.34E-21;
mr1731_2 (All); LR P-value: 2.69E-19;
mr1825_2 (All); LR P-value: 4.35E-29
LOC_Os04g41740.1 Alt: C| 5_prime_UTR_premature_start_codon_gain_variant LOW(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: C| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 79.964; most accessible tissue: Callus, score: 92.469
vg0424741090 (J) chr04 24741090 G A 52.40% 0.63% A -> G
mr1026 (All); LR P-value: 5.91E-33;
mr1063 (All); LR P-value: 1.67E-52;
mr1125 (All); LR P-value: 2.23E-48;
mr1161 (All); LR P-value: 2.29E-33;
mr1221 (All); LR P-value: 6.18E-28;
mr1260 (All); LR P-value: 8.69E-09;
mr1261 (All); LR P-value: 5.92E-16;
mr1531 (All); LR P-value: 5.97E-13;
mr1745 (All); LR P-value: 4.35E-31;
mr1914 (All); LR P-value: 5.67E-12;
mr1037_2 (All); LR P-value: 1.08E-30;
mr1094_2 (All); LR P-value: 3.92E-44;
mr1096_2 (All); LR P-value: 1.09E-59;
mr1109_2 (All); LR P-value: 1.72E-55;
mr1111_2 (All); LR P-value: 9.17E-51;
mr1121_2 (All); LR P-value: 7.53E-53;
mr1125_2 (All); LR P-value: 3.99E-65;
mr1129_2 (All); LR P-value: 3.31E-36;
mr1144_2 (All); LR P-value: 1.26E-53;
mr1208_2 (All); LR P-value: 1.80E-36;
mr1244_2 (All); LR P-value: 7.20E-25;
mr1255_2 (All); LR P-value: 1.79E-20;
mr1270_2 (All); LR P-value: 8.47E-27;
mr1457_2 (All); LR P-value: 6.96E-17;
mr1514_2 (All); LR P-value: 8.44E-13;
mr1551_2 (All); LR P-value: 3.60E-22;
mr1578_2 (All); LR P-value: 5.16E-15;
mr1690_2 (All); LR P-value: 7.29E-08;
mr1744_2 (All); LR P-value: 4.68E-16;
mr1745_2 (All); LR P-value: 5.55E-41;
mr1798_2 (All); LR P-value: 1.83E-73;
mr1913_2 (All); LR P-value: 2.88E-32;
mr1932_2 (All); LR P-value: 6.60E-30
LOC_Os04g41740.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os04g41740.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 77.868; most accessible tissue: Zhenshan97 panicle, score: 86.432
vg0424741232 (J) chr04 24741232 G A 59.90% 0.61% A -> G
mr1379 (All); LR P-value: 1.38E-09;
mr1509 (All); LR P-value: 6.58E-42;
mr1571 (All); LR P-value: 7.02E-24;
mr1580 (All); LR P-value: 9.52E-22;
mr1731 (All); LR P-value: 1.20E-24;
mr1825 (All); LR P-value: 5.54E-19;
mr1524_2 (All); LR P-value: 5.87E-06;
mr1559_2 (All); LR P-value: 3.03E-06;
mr1578_2 (All); LR P-value: 2.97E-15;
mr1580_2 (All); LR P-value: 3.32E-30;
mr1666_2 (All); LR P-value: 4.41E-12;
mr1698_2 (All); LR P-value: 2.34E-21;
mr1731_2 (All); LR P-value: 2.69E-19;
mr1825_2 (All); LR P-value: 4.35E-29
N Alt: DEL/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 76.922; most accessible tissue: Zhenshan97 flower, score: 84.217
vg0424741326 (J) chr04 24741326 T C 58.40% 0.59% C -> T
mr1509 (All); LR P-value: 6.43E-43;
mr1558 (All); LR P-value: 3.67E-46;
mr1571 (All); LR P-value: 6.99E-24;
mr1580 (All); LR P-value: 8.70E-21;
mr1731 (All); LR P-value: 2.43E-24;
mr1825 (All); LR P-value: 5.55E-18;
mr1524_2 (All); LR P-value: 9.36E-06;
mr1559_2 (All); LR P-value: 3.37E-06;
mr1578_2 (All); LR P-value: 6.02E-15
N Alt: DEL/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 76.355; most accessible tissue: Zhenshan97 panicle, score: 88.888
vg0424741333 (J) chr04 24741333 C T 94.10% 0.00% C -> T NA
LOC_Os04g41730.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: T| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 76.410; most accessible tissue: Zhenshan97 panicle, score: 89.389
vg0424741426 (J) chr04 24741426 G T 99.90% 0.00% G -> T NA
LOC_Os04g41740.1 Alt: T| missense_variant MODERATE(snpEff)
LOC_Os04g41730.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
LOC_Os04g41750.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 80.649; most accessible tissue: Zhenshan97 panicle, score: 94.026
vg0424741940 (J) chr04 24741940 G A 52.40% 0.61% A -> G
mr1026 (All); LR P-value: 2.46E-33;
mr1063 (All); LR P-value: 3.95E-54;
mr1125 (All); LR P-value: 1.86E-48;
mr1161 (All); LR P-value: 1.39E-33;
mr1164 (All); LR P-value: 9.52E-15;
mr1221 (All); LR P-value: 2.56E-28;
mr1260 (All); LR P-value: 4.20E-09;
mr1261 (All); LR P-value: 1.52E-16;
mr1531 (All); LR P-value: 1.05E-13;
mr1571 (All); LR P-value: 3.52E-23;
mr1914 (All); LR P-value: 5.67E-12;
mr1037_2 (All); LR P-value: 8.52E-31;
mr1094_2 (All); LR P-value: 3.20E-44;
mr1096_2 (All); LR P-value: 1.07E-59;
mr1109_2 (All); LR P-value: 1.71E-55;
mr1111_2 (All); LR P-value: 6.22E-51;
mr1121_2 (All); LR P-value: 3.42E-52;
mr1125_2 (All); LR P-value: 5.52E-66;
mr1129_2 (All); LR P-value: 7.75E-36;
mr1144_2 (All); LR P-value: 6.14E-54;
mr1244_2 (All); LR P-value: 5.48E-25;
mr1255_2 (All); LR P-value: 7.88E-21;
mr1457_2 (All); LR P-value: 1.16E-16;
mr1514_2 (All); LR P-value: 3.86E-13;
mr1551_2 (All); LR P-value: 1.18E-22;
mr1690_2 (All); LR P-value: 7.37E-08;
mr1744_2 (All); LR P-value: 5.12E-16;
mr1745_2 (All); LR P-value: 5.05E-41;
mr1793_2 (All); LR P-value: 5.58E-45;
mr1798_2 (All); LR P-value: 1.69E-73;
mr1913_2 (All); LR P-value: 8.55E-32;
mr1932_2 (All); LR P-value: 1.18E-29
N Alt: DEL/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: G| intron_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 84.961; most accessible tissue: Zhenshan97 panicle, score: 97.940
vg0424742100 (J) chr04 24742100 G A 95.50% 0.00% G -> A,T NA
LOC_Os04g41740.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
LOC_Os04g41740.1 Alt: T| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 87.178; most accessible tissue: Zhenshan97 panicle, score: 98.935
vg0424742142 (J) chr04 24742142 T G 55.50% 33.01% T -> G NA
LOC_Os04g41740.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os04g41740.1 Alt: G| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 88.121; most accessible tissue: Zhenshan97 panicle, score: 99.146
vg0424742197 (J) chr04 24742197 C Unkown 93.60% 2.24% C -> G NA
LOC_Os04g41740.1 Alt: G| missense_variant MODERATE(snpEff)
LOC_Os04g41730.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os04g41750.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
LOC_Os04g41759.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 94.000; most accessible tissue: Zhenshan97 panicle, score: 99.254
vg0424742305 (J) chr04 24742305 T C 52.40% 0.59% C -> T
mr1026 (All); LR P-value: 2.19E-32;
mr1063 (All); LR P-value: 9.19E-53;
mr1125 (All); LR P-value: 1.37E-48;
mr1161 (All); LR P-value: 1.39E-32;
mr1221 (All); LR P-value: 4.76E-28;
mr1260 (All); LR P-value: 4.46E-09;
mr1261 (All); LR P-value: 2.10E-16;
mr1531 (All); LR P-value: 1.26E-13;
mr1571 (All); LR P-value: 3.88E-23;
mr1914 (All); LR P-value: 2.93E-12;
mr1096_2 (All); LR P-value: 2.23E-58;
mr1109_2 (All); LR P-value: 9.24E-55;
mr1111_2 (All); LR P-value: 8.74E-50;
mr1121_2 (All); LR P-value: 6.28E-51;
mr1125_2 (All); LR P-value: 4.02E-65;
mr1144_2 (All); LR P-value: 6.13E-53;
mr1244_2 (All); LR P-value: 7.36E-25;
mr1255_2 (All); LR P-value: 1.81E-20;
mr1457_2 (All); LR P-value: 3.57E-16;
mr1514_2 (All); LR P-value: 8.15E-13;
mr1551_2 (All); LR P-value: 6.08E-23;
mr1690_2 (All); LR P-value: 4.75E-08;
mr1744_2 (All); LR P-value: 3.69E-16;
mr1745_2 (All); LR P-value: 1.86E-40;
mr1798_2 (All); LR P-value: 1.66E-72;
mr1913_2 (All); LR P-value: 1.66E-31;
mr1932_2 (All); LR P-value: 1.27E-29
LOC_Os04g41740.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os04g41740.1 Alt: T| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 94.449; most accessible tissue: Zhenshan97 panicle, score: 99.254
vg0424742486 (J) chr04 24742486 G A 59.90% 0.66% A -> G
mr1379 (All); LR P-value: 1.77E-09;
mr1509 (All); LR P-value: 8.09E-41;
mr1571 (All); LR P-value: 1.12E-23;
mr1580 (All); LR P-value: 6.32E-22;
mr1731 (All); LR P-value: 2.91E-24;
mr1825 (All); LR P-value: 4.96E-19;
mr1524_2 (All); LR P-value: 6.05E-06;
mr1559_2 (All); LR P-value: 2.89E-06;
mr1578_2 (All); LR P-value: 3.42E-15;
mr1580_2 (All); LR P-value: 2.96E-29;
mr1666_2 (All); LR P-value: 2.63E-12;
mr1698_2 (All); LR P-value: 9.69E-22
LOC_Os04g41740.1 Alt: DEL/frameshift_variant(CooVar)
LOC_Os04g41740.1 Alt: G| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)/benign(PolyPhen-2)
The average chromatin accessibility score: 90.596; most accessible tissue: Zhenshan97 panicle, score: 98.230
vg0424742515 (J) chr04 24742515 T A 99.90% 0.00% T -> A NA
LOC_Os04g41740.1 Alt: A| 3_prime_UTR_variant MODIFIER(snpEff)
LOC_Os04g41730.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os04g41750.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
LOC_Os04g41759.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)
The average chromatin accessibility score: 89.641; most accessible tissue: Zhenshan97 panicle, score: 97.798
vg0424742530 (J) chr04 24742530 C A 52.40% 0.61% A -> C
mr1063 (All); LR P-value: 5.28E-51;
mr1260 (All); LR P-value: 1.49E-08;
mr1261 (All); LR P-value: 1.62E-15;
mr1744 (All); LR P-value: 5.64E-12;
mr1745 (All); LR P-value: 8.92E-31;
mr1913 (All); LR P-value: 4.70E-17;
mr1914 (All); LR P-value: 1.10E-11;
mr1094_2 (All); LR P-value: 5.17E-45;
mr1096_2 (All); LR P-value: 1.31E-60;
mr1111_2 (All); LR P-value: 1.15E-50;
mr1121_2 (All); LR P-value: 2.50E-53;
mr1125_2 (All); LR P-value: 2.01E-63;
mr1129_2 (All); LR P-value: 1.69E-35;
mr1144_2 (All); LR P-value: 2.12E-53;
mr1244_2 (All); LR P-value: 2.85E-25;
mr1255_2 (All); LR P-value: 1.99E-20;
mr1270_2 (All); LR P-value: 2.32E-27;
mr1457_2 (All); LR P-value: 2.66E-16;
mr1551_2 (All); LR P-value: 3.31E-22;
mr1690_2 (All); LR P-value: 6.23E-08;
mr1744_2 (All); LR P-value: 3.41E-16;
mr1745_2 (All); LR P-value: 4.77E-41;
mr1798_2 (All); LR P-value: 8.39E-72;
mr1913_2 (All); LR P-value: 2.92E-32;
mr1932_2 (All); LR P-value: 8.92E-30
LOC_Os04g41740.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
N Alt: DEL/silent_mutation(CooVar)
The average chromatin accessibility score: 89.463; most accessible tissue: Zhenshan97 panicle, score: 97.556
vg0424742629 (J) chr04 24742629 TTA T 94.00% 0.04% TTA -> T NA
N Alt: DEL/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 76.860; most accessible tissue: Zhenshan97 root, score: 94.300
vg0424742630 (J) chr04 24742630 T TA 53.50% 0.57% TA -> T NA
N Alt: DEL/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: T| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: T| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 76.742; most accessible tissue: Zhenshan97 root, score: 94.256
vg0424742654 (J) chr04 24742654 T TCTATC 98.20% 0.00% T -> TCTATTA,TC TATC,TCTAT CTATTATATA ATTAAAGGAA ,TCTATCTAT TA,TCTATTA TATAATTAAA GGAA,TCTAT CTATTATA NA
LOC_Os04g41740.1 Alt: TCTATCTATTATATAATTAAAGGAA| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: TCTATCTATTATATAATTAAAGGAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: TCTATCTATTATATAATTAAAGGAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: TCTATCTATTATATAATTAAAGGAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: TCTATCTATTATA| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: TCTATCTATTATA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: TCTATCTATTATA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: TCTATCTATTATA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: TCTATC| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: TCTATC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: TCTATC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: TCTATC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: TCTATCTATTA| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: TCTATCTATTA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: TCTATCTATTA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: TCTATCTATTA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: TCTATTA| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: TCTATTA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: TCTATTA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: TCTATTA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41740.1 Alt: TCTATTATATAATTAAAGGAA| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41730.1 Alt: TCTATTATATAATTAAAGGAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41750.1 Alt: TCTATTATATAATTAAAGGAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os04g41759.1 Alt: TCTATTATATAATTAAAGGAA| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar)
The average chromatin accessibility score: 71.121; most accessible tissue: Minghui63 root, score: 92.448
STR0424742623 (J) chr04 24742623 TTT TT 59.00% 0.00% TTTT -> TT,TTT NA