Variant report
| Variant | rs7934467 |
|---|---|
| Chromosome Location | chr11:93635203-93635204 |
| 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 |
rSNPs within LD-proxies of this variant (count:33)
| rs_ID | r2[population] |
|---|---|
| rs12785450 | 0.83[ASN][1000 genomes] |
| rs12806242 | 0.83[ASN][1000 genomes] |
| rs1573567 | 0.89[EUR][1000 genomes] |
| rs16919533 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
| rs16919815 | 1.00[CHB][hapmap] |
| rs55659547 | 0.83[ASN][1000 genomes] |
| rs56359140 | 0.83[ASN][1000 genomes] |
| rs57856352 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs60351354 | 0.89[EUR][1000 genomes] |
| rs60546087 | 0.89[EUR][1000 genomes] |
| rs60550219 | 0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
| rs67167563 | 0.89[EUR][1000 genomes];0.83[ASN][1000 genomes] |
| rs67232024 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs67549397 | 0.89[EUR][1000 genomes] |
| rs67812366 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs67915626 | 0.83[ASN][1000 genomes] |
| rs7102422 | 0.83[ASN][1000 genomes] |
| rs7105405 | 0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
| rs7109132 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7109819 | 0.89[EUR][1000 genomes] |
| rs71480693 | 0.83[ASN][1000 genomes] |
| rs72962860 | 0.83[ASN][1000 genomes] |
| rs72962872 | 0.83[ASN][1000 genomes] |
| rs72962880 | 0.83[ASN][1000 genomes] |
| rs72962891 | 0.83[ASN][1000 genomes] |
| rs7927828 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7932290 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7941015 | 0.83[ASN][1000 genomes] |
| rs7950356 | 0.83[ASN][1000 genomes] |
| rs950878 | 0.87[EUR][1000 genomes];0.83[ASN][1000 genomes] |
| rs9888143 | 0.89[EUR][1000 genomes] |
| rs9888156 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
| rs9888266 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv898181 | chr11:93072843-93662459 | Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 119 gene(s) | inside rSNPs | diseases |
| 2 | nsv898182 | chr11:93381845-93637462 | Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 108 gene(s) | inside rSNPs | diseases |
| 3 | nsv508650 | chr11:93609010-93713576 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
mRNA abundance (count:1)
| SNP | Gene | Cis/trans | Tissue | Source |
|---|---|---|---|---|
| rs7934467 | HEPHL1 | cis | Artery Tibial | GTEx |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:93634400-93638400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 2 | chr11:93635200-93635800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
