Variant report
| Variant | rs12663695 |
|---|---|
| Chromosome Location | chr6:74085810-74085811 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:3 , 50 per page) page:
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| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000234882 | Chromatin interaction |
| ENSG00000135297 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:15)
| rs_ID | r2[population] |
|---|---|
| rs11961187 | 0.90[AMR][1000 genomes] |
| rs11964808 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
| rs12662148 | 0.86[CHB][hapmap];0.90[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[ASN][1000 genomes] |
| rs12665048 | 0.86[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.87[ASN][1000 genomes] |
| rs16883692 | 0.86[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes] |
| rs2280286 | 0.87[AMR][1000 genomes] |
| rs3734512 | 0.85[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.87[ASN][1000 genomes] |
| rs3734516 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[ASN][1000 genomes] |
| rs3757107 | 0.86[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.87[ASN][1000 genomes] |
| rs723402 | 0.94[AMR][1000 genomes];0.87[ASN][1000 genomes] |
| rs72961942 | 1.00[AFR][1000 genomes] |
| rs7747491 | 0.85[AMR][1000 genomes] |
| rs930806 | 0.86[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs930807 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes] |
| rs930808 | 0.94[AMR][1000 genomes];0.87[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | esv3410973 | chr6:73716033-74419545 | Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 191 gene(s) | inside rSNPs | diseases |
| 2 | nsv830693 | chr6:74049342-74216080 | Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
| 3 | nsv969419 | chr6:74082277-74086772 | ZNF genes & repeats Weak transcription Enhancers | TF binding regionChromatin interactive region | 4 gene(s) | inside rSNPs | n/a |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
