Variant report
Variant | rs9459871 |
---|---|
Chromosome Location | chr6:167499092-167499093 |
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] |
---|---|
rs10946205 | 0.80[ASN][1000 genomes] |
rs10946208 | 0.86[EUR][1000 genomes] |
rs12203510 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12213683 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12523712 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12527827 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12528323 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12528689 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12529238 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12529876 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12529959 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs13199692 | 0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13208636 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs13210649 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs13213249 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs1358882 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1358883 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1407315 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17615336 | 0.83[AMR][1000 genomes] |
rs1810644 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1810645 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs2001114 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs2001115 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2017338 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs204295 | 0.89[ASN][1000 genomes] |
rs2181058 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2239826 | 0.82[AMR][1000 genomes] |
rs2285147 | 0.80[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs2285148 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4710176 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs62436765 | 0.81[EUR][1000 genomes] |
rs6456149 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6456150 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6456151 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6456153 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs6456154 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs6902119 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6909180 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs6909475 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs6909502 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6918286 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6921588 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6925969 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6932740 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6934043 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6936261 | 0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6941355 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs720325 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7742305 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7748224 | 0.83[EUR][1000 genomes] |
rs7760495 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7761977 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7762156 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs911632 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9457261 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9457268 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9459853 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9459862 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9459870 | 0.85[EUR][1000 genomes] |
rs9459872 | 0.83[AMR][1000 genomes] |
rs9459874 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1019381 | chr6:167090236-167558598 | Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv538541 | chr6:167090236-167558598 | Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv948634 | chr6:167200671-167838993 | Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 25 gene(s) | inside rSNPs | diseases |
4 | nsv532074 | chr6:167320656-167781977 | Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 23 gene(s) | inside rSNPs | diseases |
5 | nsv1031039 | chr6:167324021-167741439 | Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 21 gene(s) | inside rSNPs | diseases |
6 | nsv538543 | chr6:167324021-167741439 | Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 21 gene(s) | inside rSNPs | diseases |
7 | nsv1026972 | chr6:167335031-167671042 | Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
8 | nsv886943 | chr6:167440244-167502638 | Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
9 | esv2752099 | chr6:167448181-167579102 | Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
10 | nsv1018193 | chr6:167491589-167797294 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
11 | nsv538544 | chr6:167491589-167797294 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:167492000-167503400 | Weak transcription | Right Atrium | heart |