Variant report
| Variant | rs35070061 |
|---|---|
| Chromosome Location | chr12:26033499-26033500 |
| allele | G/T |
| 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] |
|---|---|
| rs10842632 | 0.90[ASN][1000 genomes] |
| rs11048327 | 0.90[ASN][1000 genomes] |
| rs11048332 | 0.88[ASN][1000 genomes] |
| rs11048333 | 0.87[ASN][1000 genomes] |
| rs11048334 | 0.86[ASN][1000 genomes] |
| rs11048335 | 0.81[ASN][1000 genomes] |
| rs12422269 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs12427059 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs12812530 | 0.85[EUR][1000 genomes] |
| rs12816906 | 0.88[ASN][1000 genomes] |
| rs12817333 | 0.87[ASN][1000 genomes] |
| rs12824703 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
| rs12831978 | 0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs2342372 | 0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs34253073 | 0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
| rs34704732 | 0.88[EUR][1000 genomes] |
| rs34810288 | 0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs34878109 | 0.88[ASN][1000 genomes] |
| rs35642650 | 0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
| rs35972516 | 0.83[EUR][1000 genomes] |
| rs66485863 | 0.85[EUR][1000 genomes] |
| rs67678522 | 0.85[EUR][1000 genomes] |
| rs73084200 | 0.85[EUR][1000 genomes] |
| rs73086129 | 0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs73086133 | 0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs73088119 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[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 | esv2758300 | chr12:25992331-26161116 | Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 38 gene(s) | inside rSNPs | diseases |
| 2 | esv2759886 | chr12:25992331-26161116 | Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 38 gene(s) | inside rSNPs | diseases |
| 3 | nsv1035319 | chr12:26020667-26097148 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers | TF binding regionChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
| 4 | nsv528977 | chr12:26033286-26034653 | Weak transcription | n/a | n/a | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:26028600-26034800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
