Variant report
| Variant | rs4645374 |
|---|---|
| Chromosome Location | chr5:108612057-108612058 |
| 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 |
rSNPs within LD-proxies of this variant (count:29)
| rs_ID | r2[population] |
|---|---|
| rs10070978 | 0.93[ASN][1000 genomes] |
| rs10078014 | 0.92[ASN][1000 genomes] |
| rs1118708 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs12515174 | 0.88[ASN][1000 genomes] |
| rs12518496 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
| rs12520021 | 1.00[ASN][1000 genomes] |
| rs12520951 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
| rs12522411 | 1.00[ASN][1000 genomes] |
| rs1363214 | 0.86[ASN][1000 genomes] |
| rs1422003 | 0.89[ASN][1000 genomes] |
| rs17473588 | 0.92[ASN][1000 genomes] |
| rs4346815 | 0.81[ASN][1000 genomes] |
| rs57331834 | 0.83[EUR][1000 genomes] |
| rs57400924 | 0.92[ASN][1000 genomes] |
| rs60496657 | 1.00[ASN][1000 genomes] |
| rs62376832 | 0.84[ASN][1000 genomes] |
| rs6864796 | 0.92[ASN][1000 genomes] |
| rs6866668 | 0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs6877495 | 0.92[ASN][1000 genomes] |
| rs6881141 | 0.92[ASN][1000 genomes] |
| rs6884332 | 0.86[ASN][1000 genomes] |
| rs6899020 | 1.00[ASN][1000 genomes] |
| rs7700949 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7715416 | 0.96[ASN][1000 genomes] |
| rs7716124 | 0.93[ASN][1000 genomes] |
| rs7718897 | 0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes] |
| rs7720237 | 1.00[ASN][1000 genomes] |
| rs7727900 | 0.92[ASN][1000 genomes] |
| rs9968753 | 0.81[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1027163 | chr5:108445447-108839913 | Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
| 2 | nsv599338 | chr5:108528729-108675737 | Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| 3 | nsv508375 | chr5:108587628-108624046 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 4 | esv2763481 | chr5:108605390-108693696 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:108601800-108615000 | Weak transcription | Pancreas | Pancrea |
| 2 | chr5:108611800-108612200 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
