Variant report
| Variant | rs7146571 |
|---|---|
| Chromosome Location | chr14:82091744-82091745 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:39)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:39 , 50 per page) page:
1
| No data |
(count:2 , 50 per page) page:
1
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000258977 | TF binding region |
rSNPs within LD-proxies of this variant (count:18)
| rs_ID | r2[population] |
|---|---|
| rs11846543 | 1.00[EUR][1000 genomes] |
| rs11849848 | 1.00[EUR][1000 genomes] |
| rs11851708 | 1.00[EUR][1000 genomes] |
| rs11851769 | 1.00[EUR][1000 genomes] |
| rs11851776 | 1.00[EUR][1000 genomes] |
| rs17115917 | 1.00[EUR][1000 genomes] |
| rs56171233 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs57506135 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs57578871 | 1.00[EUR][1000 genomes] |
| rs59877625 | 1.00[EUR][1000 genomes] |
| rs59911720 | 1.00[EUR][1000 genomes] |
| rs6574682 | 1.00[EUR][1000 genomes] |
| rs7148848 | 1.00[EUR][1000 genomes] |
| rs7154704 | 1.00[EUR][1000 genomes] |
| rs7156396 | 1.00[EUR][1000 genomes] |
| rs7156980 | 1.00[EUR][1000 genomes] |
| rs8011500 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs8022831 | 1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1047694 | chr14:81831147-82534026 | Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
| 2 | nsv542145 | chr14:81831147-82534026 | Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
| 3 | nsv565299 | chr14:81983027-82586324 | Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
| 4 | nsv1052666 | chr14:82069162-83028382 | Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
| 5 | nsv902121 | chr14:82075469-82146538 | Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:82088400-82095600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
