Variant report
| Variant | rs11475834 |
|---|---|
| Chromosome Location | chr8:110509679-110509680 |
| allele | -/T |
| 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:
1
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000235010 | Chromatin interaction |
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 | nsv891281 | chr8:110450092-110558622 | Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
| 2 | esv2554092 | chr8:110509394-110511181 | Inactive region | TF binding regionChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| 3 | esv3428944 | chr8:110509626-110511624 | Inactive region | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| 4 | esv1361780 | chr8:110509678-110509679 | Inactive region | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| 5 | nsv369725 | chr8:110509679-110509679 | Inactive region | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
