Variant report
| Variant | rs540531507 |
|---|---|
| Chromosome Location | chr1:84515630-84515631 |
| allele | A/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:
1
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000142875 | Chromatin interaction |
| ENSG00000271576 | Chromatin interaction |
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 | nsv1732 | chr1:84499098-84544635 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
| 2 | nsv508360 | chr1:84500230-84524997 | Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| 3 | esv3498832 | chr1:84514725-84525109 | Enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
| 4 | esv3498833 | chr1:84514725-84525109 | Enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
