Variant report
Variant | rs3134179 |
---|---|
Chromosome Location | chr8:100351568-100351569 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10098138 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10112186 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10808361 | 0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10955204 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10955206 | 0.86[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10955207 | 0.81[EUR][1000 genomes] |
rs11773983 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs11784152 | 0.84[EUR][1000 genomes] |
rs11988987 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11989177 | 0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11992517 | 0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12056311 | 0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12234903 | 0.81[EUR][1000 genomes] |
rs12549438 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12678371 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs13250430 | 0.86[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13250549 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs13265237 | 0.85[AMR][1000 genomes] |
rs13271726 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1492077 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1565581 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1989645 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs2029595 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2029596 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2046936 | 0.81[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs28617503 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs3103697 | 0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3103708 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3103709 | 0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3103715 | 0.82[EUR][1000 genomes] |
rs3103716 | 0.80[EUR][1000 genomes] |
rs3103718 | 0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs3103719 | 0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs3103722 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3103728 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3103729 | 0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3103731 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3105167 | 0.82[EUR][1000 genomes] |
rs3105179 | 0.82[EUR][1000 genomes] |
rs3105182 | 0.83[EUR][1000 genomes] |
rs3105183 | 0.83[EUR][1000 genomes] |
rs3105184 | 0.83[EUR][1000 genomes] |
rs3105188 | 0.80[EUR][1000 genomes] |
rs3105189 | 0.80[EUR][1000 genomes] |
rs3110395 | 0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3110397 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3110398 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs3110403 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3134159 | 0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs3134172 | 0.84[EUR][1000 genomes] |
rs3134174 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3134177 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3134178 | 0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3134298 | 0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs3134299 | 0.84[EUR][1000 genomes] |
rs3134302 | 0.82[EUR][1000 genomes] |
rs3134304 | 0.80[EUR][1000 genomes] |
rs3134307 | 0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3890706 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4338069 | 0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4366054 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4490802 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4517095 | 0.81[AMR][1000 genomes] |
rs4734426 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4735600 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4735601 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs5019794 | 0.84[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs55893057 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs58752318 | 0.86[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs60042922 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6468660 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs6468661 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6468664 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6468668 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6468670 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6468673 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6468674 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6468677 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6468678 | 0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6468679 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6651157 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6988226 | 0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6999062 | 0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6999263 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7010581 | 0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7010582 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7011067 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7012312 | 0.84[AMR][1000 genomes] |
rs7014877 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs716454 | 1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs72670298 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72670300 | 0.83[EUR][1000 genomes] |
rs7341678 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7459833 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7460625 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7461615 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7463462 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7464318 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7464742 | 0.83[AMR][1000 genomes] |
rs7464775 | 0.85[AMR][1000 genomes] |
rs7465566 | 0.85[AMR][1000 genomes] |
rs7816323 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7816673 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7816843 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7818037 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7823291 | 0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7826207 | 0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7828262 | 0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7832772 | 0.86[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7832780 | 0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7837218 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7837937 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7844283 | 0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9297288 | 0.80[EUR][1000 genomes] |
rs957539 | 0.84[EUR][1000 genomes] |
rs9774546 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs9792181 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1031089 | chr8:99715785-100399935 | Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
2 | nsv531505 | chr8:99932947-100464147 | Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
3 | nsv524617 | chr8:100032844-100717925 | ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
4 | nsv1020614 | chr8:100046692-100594092 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
5 | nsv1026442 | chr8:100075230-100561451 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
6 | nsv539694 | chr8:100075230-100561451 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
7 | nsv821659 | chr8:100147641-100369829 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
8 | nsv1022914 | chr8:100190356-100720313 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
9 | nsv539695 | chr8:100190356-100720313 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
10 | nsv1031524 | chr8:100204139-100399935 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
11 | nsv933080 | chr8:100204936-100417432 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
12 | nsv611812 | chr8:100232372-100464671 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
13 | nsv1027031 | chr8:100250184-100442195 | Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
14 | nsv539696 | chr8:100250184-100442195 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
15 | nsv933677 | chr8:100254133-100455039 | Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
16 | nsv831407 | chr8:100284406-100448725 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
17 | nsv1031100 | chr8:100290887-100508952 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
18 | nsv539697 | chr8:100290887-100508952 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
19 | nsv529685 | chr8:100290888-100463947 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
20 | nsv891226 | chr8:100295634-100708595 | Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 15 gene(s) | inside rSNPs | diseases |
21 | nsv891227 | chr8:100295634-100743556 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 15 gene(s) | inside rSNPs | diseases |
22 | nsv1019168 | chr8:100324341-100361194 | Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
23 | nsv1019256 | chr8:100336249-100852803 | Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
24 | nsv539698 | chr8:100336249-100852803 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:100326400-100354600 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
2 | chr8:100327000-100361800 | Weak transcription | Aorta | Aorta |
3 | chr8:100334600-100352800 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr8:100339800-100351600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
5 | chr8:100340800-100351600 | Weak transcription | Primary monocytes fromperipheralblood | blood |
6 | chr8:100346200-100361400 | Weak transcription | Primary T cells from cord blood | blood |
7 | chr8:100346400-100354800 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
8 | chr8:100346600-100362800 | Weak transcription | Primary B cells from cord blood | blood |
9 | chr8:100350200-100359800 | Weak transcription | Left Ventricle | heart |
10 | chr8:100350600-100365600 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
11 | chr8:100351200-100353600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |