Variant report
Variant | rs13279413 |
---|---|
Chromosome Location | chr8:52588083-52588084 |
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] |
---|---|
rs10088109 | 0.91[ASN][1000 genomes] |
rs10090123 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs10090972 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10091454 | 0.86[EUR][1000 genomes] |
rs10101657 | 0.91[ASN][1000 genomes] |
rs10106091 | 0.87[EUR][1000 genomes] |
rs10109862 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10112473 | 0.91[ASN][1000 genomes] |
rs10113743 | 0.91[ASN][1000 genomes] |
rs10958295 | 0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs10958296 | 0.87[EUR][1000 genomes] |
rs10958297 | 0.81[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs12541234 | 0.88[ASN][1000 genomes] |
rs12549383 | 0.88[ASN][1000 genomes] |
rs12678094 | 0.88[ASN][1000 genomes] |
rs1317774 | 0.91[EUR][1000 genomes] |
rs13251959 | 0.83[EUR][1000 genomes] |
rs13251960 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13252521 | 0.88[ASN][1000 genomes] |
rs13259819 | 0.91[ASN][1000 genomes] |
rs13268396 | 0.81[EUR][1000 genomes] |
rs13268711 | 0.82[EUR][1000 genomes] |
rs13270001 | 0.85[EUR][1000 genomes] |
rs13274101 | 0.82[EUR][1000 genomes] |
rs13277004 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs13439031 | 0.88[ASN][1000 genomes] |
rs16916741 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs16916756 | 0.82[EUR][1000 genomes] |
rs16916763 | 0.83[EUR][1000 genomes] |
rs28512421 | 0.86[EUR][1000 genomes] |
rs28549751 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28616568 | 0.86[EUR][1000 genomes] |
rs2976204 | 0.88[ASN][1000 genomes] |
rs2976209 | 0.87[EUR][1000 genomes] |
rs34342438 | 0.86[EUR][1000 genomes] |
rs34773755 | 0.88[ASN][1000 genomes] |
rs35153909 | 0.83[EUR][1000 genomes] |
rs35195931 | 0.86[EUR][1000 genomes] |
rs35326600 | 0.88[ASN][1000 genomes] |
rs36075262 | 0.80[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4242472 | 0.82[EUR][1000 genomes] |
rs4275221 | 0.82[EUR][1000 genomes] |
rs4326377 | 0.84[EUR][1000 genomes] |
rs4382468 | 0.91[ASN][1000 genomes] |
rs4397396 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs4400372 | 0.87[EUR][1000 genomes] |
rs4407875 | 0.91[ASN][1000 genomes] |
rs4421345 | 0.91[ASN][1000 genomes] |
rs4541902 | 0.85[ASN][1000 genomes] |
rs4621801 | 0.89[ASN][1000 genomes] |
rs4873200 | 0.91[ASN][1000 genomes] |
rs4873201 | 0.84[EUR][1000 genomes] |
rs4873570 | 0.83[ASN][1000 genomes] |
rs4873571 | 0.91[ASN][1000 genomes] |
rs4873572 | 0.88[EUR][1000 genomes] |
rs4873573 | 0.83[EUR][1000 genomes] |
rs4873575 | 0.86[EUR][1000 genomes] |
rs4873576 | 0.88[ASN][1000 genomes] |
rs4873584 | 0.81[EUR][1000 genomes] |
rs5000332 | 0.91[ASN][1000 genomes] |
rs55701628 | 0.86[EUR][1000 genomes] |
rs6473637 | 0.91[ASN][1000 genomes] |
rs6473638 | 0.91[ASN][1000 genomes] |
rs6981260 | 0.87[EUR][1000 genomes] |
rs6986571 | 0.87[EUR][1000 genomes] |
rs6986605 | 0.87[EUR][1000 genomes] |
rs6988401 | 0.91[ASN][1000 genomes] |
rs6999693 | 0.87[EUR][1000 genomes] |
rs7005788 | 0.87[EUR][1000 genomes] |
rs7007671 | 0.88[EUR][1000 genomes] |
rs7007741 | 1.00[ASN][1000 genomes] |
rs7007804 | 0.81[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7011666 | 0.86[EUR][1000 genomes] |
rs7012655 | 0.80[ASN][1000 genomes] |
rs7014372 | 0.87[ASN][1000 genomes] |
rs7830013 | 0.88[ASN][1000 genomes] |
rs7839661 | 0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8180923 | 0.83[ASN][1000 genomes] |
rs9284000 | 0.91[ASN][1000 genomes] |
rs9643788 | 0.80[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9650303 | 0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv932026 | chr8:51858658-52758574 | Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
2 | nsv890895 | chr8:52190571-52615191 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv817615 | chr8:52252405-53023384 | Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
4 | nsv1018429 | chr8:52411443-52878946 | Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
5 | nsv1034856 | chr8:52411443-52886765 | Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
6 | nsv831313 | chr8:52458835-52638968 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv890898 | chr8:52579964-52680933 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:52580800-52598800 | Weak transcription | Right Atrium | heart |
2 | chr8:52583400-52589000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr8:52585000-52595000 | Weak transcription | Left Ventricle | heart |
4 | chr8:52586600-52588600 | Weak transcription | Fetal Lung | lung |