Variant report
| Variant | rs7630218 |
|---|---|
| Chromosome Location | chr3:34168049-34168050 |
| 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:26)
| rs_ID | r2[population] |
|---|---|
| rs1002489 | 0.91[ASN][1000 genomes] |
| rs12489252 | 0.81[AMR][1000 genomes] |
| rs12494669 | 0.98[ASN][1000 genomes] |
| rs12495732 | 0.91[ASN][1000 genomes] |
| rs12638888 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
| rs13062392 | 0.91[ASN][1000 genomes] |
| rs1440382 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
| rs1440387 | 0.81[ASN][1000 genomes] |
| rs1561594 | 0.98[ASN][1000 genomes] |
| rs1583821 | 0.97[ASN][1000 genomes] |
| rs1899082 | 0.95[ASN][1000 genomes] |
| rs2099753 | 0.91[ASN][1000 genomes] |
| rs2218183 | 0.91[ASN][1000 genomes] |
| rs4044970 | 0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
| rs4678459 | 0.81[AMR][1000 genomes];0.82[ASN][1000 genomes] |
| rs4678651 | 0.88[ASN][1000 genomes] |
| rs6801432 | 0.81[AMR][1000 genomes];0.81[ASN][1000 genomes] |
| rs7614971 | 0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
| rs7631478 | 0.89[ASN][1000 genomes] |
| rs7633784 | 0.88[ASN][1000 genomes] |
| rs7641622 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7643151 | 0.90[ASN][1000 genomes] |
| rs7653017 | 0.81[AMR][1000 genomes];0.81[ASN][1000 genomes] |
| rs893923 | 0.91[ASN][1000 genomes] |
| rs9835388 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes] |
| rs9852942 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[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 | nsv522881 | chr3:33736126-34241686 | Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
| 2 | nsv1001599 | chr3:34149575-34437701 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| 3 | nsv536533 | chr3:34149575-34437701 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| 4 | nsv876682 | chr3:34149814-34401451 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:34168000-34168200 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
