Variant report
Variant | rs73448558 |
---|---|
Chromosome Location | chr18:39503301-39503302 |
allele | A/C |
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] |
---|---|
rs1142044 | 1.00[EUR][1000 genomes] |
rs11873469 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11873602 | 1.00[EUR][1000 genomes] |
rs11874766 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11874775 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11874814 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11874830 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11876547 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11876578 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11877901 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1540057 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16975441 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16975447 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16975463 | 1.00[EUR][1000 genomes] |
rs16975466 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16975521 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2469471 | 1.00[EUR][1000 genomes] |
rs490578 | 1.00[EUR][1000 genomes] |
rs493100 | 1.00[EUR][1000 genomes] |
rs525369 | 1.00[EUR][1000 genomes] |
rs542870 | 1.00[EUR][1000 genomes] |
rs55655849 | 1.00[EUR][1000 genomes] |
rs563840 | 1.00[EUR][1000 genomes] |
rs56411890 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56751463 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56979511 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57208863 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs575366 | 1.00[EUR][1000 genomes] |
rs58298297 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs583163 | 1.00[EUR][1000 genomes] |
rs58390786 | 1.00[EUR][1000 genomes] |
rs584022 | 1.00[EUR][1000 genomes] |
rs586797 | 1.00[EUR][1000 genomes] |
rs58881642 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs591870 | 1.00[EUR][1000 genomes] |
rs593689 | 1.00[EUR][1000 genomes] |
rs606366 | 1.00[EUR][1000 genomes] |
rs608428 | 1.00[EUR][1000 genomes] |
rs616575 | 1.00[EUR][1000 genomes] |
rs633541 | 1.00[EUR][1000 genomes] |
rs635560 | 1.00[EUR][1000 genomes] |
rs640064 | 1.00[EUR][1000 genomes] |
rs640460 | 1.00[EUR][1000 genomes] |
rs643772 | 1.00[EUR][1000 genomes] |
rs645148 | 1.00[EUR][1000 genomes] |
rs647084 | 1.00[EUR][1000 genomes] |
rs6507453 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6507454 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs655693 | 1.00[EUR][1000 genomes] |
rs659950 | 1.00[EUR][1000 genomes] |
rs6650669 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs669235 | 1.00[EUR][1000 genomes] |
rs670429 | 1.00[EUR][1000 genomes] |
rs674380 | 1.00[EUR][1000 genomes] |
rs684091 | 1.00[EUR][1000 genomes] |
rs7229485 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7237185 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7237815 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7238919 | 1.00[EUR][1000 genomes] |
rs7239880 | 1.00[EUR][1000 genomes] |
rs7240066 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7241399 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7242077 | 1.00[EUR][1000 genomes] |
rs7245131 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7343027 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73451096 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73452235 | 1.00[EUR][1000 genomes] |
rs73452297 | 1.00[EUR][1000 genomes] |
rs73452300 | 1.00[EUR][1000 genomes] |
rs73453013 | 1.00[EUR][1000 genomes] |
rs73454552 | 1.00[EUR][1000 genomes] |
rs73454573 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73454580 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73454581 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73454593 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73454596 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73454602 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73950814 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8084037 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8085708 | 1.00[EUR][1000 genomes] |
rs8088187 | 0.87[AMR][1000 genomes] |
rs8089142 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8090403 | 1.00[EUR][1000 genomes] |
rs8095945 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9948650 | 1.00[EUR][1000 genomes] |
rs9965647 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1066869 | chr18:38742896-39680723 | Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | nsv543685 | chr18:38742896-39680723 | Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
3 | nsv949609 | chr18:39126941-40070286 | Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 11 gene(s) | inside rSNPs | diseases |
4 | nsv431979 | chr18:39255558-39696452 | Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
5 | nsv1066029 | chr18:39322920-39623625 | Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv543686 | chr18:39322920-39623625 | Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv909566 | chr18:39327962-39688452 | Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
8 | esv34153 | chr18:39398768-39872265 | Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
9 | nsv909567 | chr18:39470190-39652939 | Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
10 | nsv2268 | chr18:39487042-39531721 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
11 | nsv909568 | chr18:39491873-39768746 | Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:39501600-39504000 | Enhancers | Fetal Lung | lung |
2 | chr18:39502000-39503600 | Enhancers | Fetal Kidney | kidney |
3 | chr18:39503200-39504200 | Enhancers | Primary monocytes fromperipheralblood | blood |