Variant report
| Variant | rs35900434 |
|---|---|
| Chromosome Location | chr6:54550513-54550514 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:2 , 50 per page) page:
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| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000168143 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:9)
| rs_ID | r2[population] |
|---|---|
| rs34282556 | 0.90[EUR][1000 genomes] |
| rs34850008 | 0.95[AFR][1000 genomes] |
| rs35389705 | 0.92[AFR][1000 genomes];0.86[ASN][1000 genomes] |
| rs35749125 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs35767679 | 0.95[AFR][1000 genomes] |
| rs58221645 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
| rs71558893 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
| rs71558894 | 0.90[EUR][1000 genomes] |
| rs7750348 | 0.87[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv885900 | chr6:54517968-54852462 | Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
| 2 | esv1813954 | chr6:54518364-54557296 | Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
