Variant report
Variant | rs34464472 |
---|---|
Chromosome Location | chr11:104674625-104674626 |
allele | -/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] |
---|---|
rs12276274 | 1.00[EUR][1000 genomes] |
rs12286054 | 1.00[EUR][1000 genomes] |
rs17093742 | 1.00[AMR][1000 genomes] |
rs17102890 | 1.00[AMR][1000 genomes] |
rs17103039 | 1.00[AMR][1000 genomes] |
rs17103106 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17103307 | 1.00[EUR][1000 genomes] |
rs17103313 | 1.00[EUR][1000 genomes] |
rs2114368 | 1.00[EUR][1000 genomes] |
rs2114369 | 1.00[EUR][1000 genomes] |
rs2114370 | 1.00[EUR][1000 genomes] |
rs2162342 | 1.00[EUR][1000 genomes] |
rs3181337 | 1.00[AMR][1000 genomes] |
rs3888096 | 1.00[EUR][1000 genomes] |
rs4258348 | 1.00[EUR][1000 genomes] |
rs4540818 | 1.00[EUR][1000 genomes] |
rs477993 | 1.00[EUR][1000 genomes] |
rs482385 | 1.00[EUR][1000 genomes] |
rs484438 | 1.00[EUR][1000 genomes] |
rs5000899 | 1.00[EUR][1000 genomes] |
rs508916 | 1.00[EUR][1000 genomes] |
rs517153 | 1.00[EUR][1000 genomes] |
rs520766 | 1.00[EUR][1000 genomes] |
rs521107 | 1.00[EUR][1000 genomes] |
rs525020 | 1.00[EUR][1000 genomes] |
rs527522 | 1.00[EUR][1000 genomes] |
rs530398 | 1.00[EUR][1000 genomes] |
rs532089 | 1.00[EUR][1000 genomes] |
rs550051 | 1.00[EUR][1000 genomes] |
rs556062 | 1.00[EUR][1000 genomes] |
rs556589 | 1.00[EUR][1000 genomes] |
rs557069 | 1.00[EUR][1000 genomes] |
rs566945 | 1.00[EUR][1000 genomes] |
rs579353 | 1.00[EUR][1000 genomes] |
rs59301970 | 1.00[EUR][1000 genomes] |
rs606399 | 1.00[EUR][1000 genomes] |
rs608655 | 1.00[EUR][1000 genomes] |
rs619515 | 1.00[EUR][1000 genomes] |
rs626354 | 1.00[EUR][1000 genomes] |
rs640857 | 1.00[EUR][1000 genomes] |
rs652377 | 1.00[EUR][1000 genomes] |
rs655884 | 1.00[EUR][1000 genomes] |
rs693506 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1046098 | chr11:104207210-105003661 | Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
2 | nsv1054456 | chr11:104358924-104805251 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv531430 | chr11:104380924-105194452 | Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
4 | nsv826072 | chr11:104662708-104768357 | Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:104674400-104674800 | Flanking Active TSS | Dnd41 | blood |
2 | chr11:104674400-104675000 | Enhancers | GM12878-XiMat | blood |
3 | chr11:104674600-104675000 | Enhancers | Primary monocytes fromperipheralblood | blood |