Variant report
| Variant | rs73514228 |
|---|---|
| Chromosome Location | chr9:96664657-96664658 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:4 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr9:96664499..96666537-chr9:96711318..96713769,2 | MCF-7 | breast: | |
| 2 | chr9:96655426..96659394-chr9:96661426..96665501,6 | MCF-7 | breast: | |
| 3 | chr9:96662639..96665282-chr9:96667242..96668877,2 | K562 | blood: | |
| 4 | chr9:96619287..96621506-chr9:96664361..96666949,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000231990 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:33)
| rs_ID | r2[population] |
|---|---|
| rs56948438 | 1.00[AMR][1000 genomes] |
| rs57233442 | 1.00[AMR][1000 genomes] |
| rs58181103 | 1.00[AMR][1000 genomes] |
| rs58459148 | 1.00[AMR][1000 genomes] |
| rs58709329 | 1.00[AMR][1000 genomes] |
| rs59050355 | 1.00[AMR][1000 genomes] |
| rs59264265 | 1.00[AMR][1000 genomes] |
| rs59541311 | 1.00[AMR][1000 genomes] |
| rs59630172 | 1.00[AMR][1000 genomes] |
| rs60051875 | 1.00[AMR][1000 genomes] |
| rs60230389 | 1.00[AMR][1000 genomes] |
| rs60470247 | 1.00[AMR][1000 genomes] |
| rs61384012 | 1.00[AMR][1000 genomes] |
| rs73512601 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs73514235 | 1.00[AMR][1000 genomes] |
| rs73514244 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs73516177 | 1.00[AMR][1000 genomes] |
| rs73516179 | 1.00[AMR][1000 genomes] |
| rs73516279 | 1.00[AMR][1000 genomes] |
| rs73516289 | 1.00[AMR][1000 genomes] |
| rs73516290 | 1.00[AMR][1000 genomes] |
| rs73517142 | 1.00[AMR][1000 genomes] |
| rs73517166 | 1.00[AMR][1000 genomes] |
| rs73517183 | 1.00[AMR][1000 genomes] |
| rs73517184 | 1.00[AMR][1000 genomes] |
| rs73518259 | 1.00[AMR][1000 genomes] |
| rs73518278 | 1.00[AMR][1000 genomes] |
| rs73518291 | 1.00[AMR][1000 genomes] |
| rs73519488 | 1.00[AMR][1000 genomes] |
| rs73520278 | 1.00[AMR][1000 genomes] |
| rs73520282 | 1.00[AMR][1000 genomes] |
| rs73521324 | 1.00[AMR][1000 genomes] |
| rs73521348 | 1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv893588 | chr9:96620419-96668352 | Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| 2 | nsv893589 | chr9:96624645-96884544 | Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
| 3 | nsv1053137 | chr9:96644876-96683214 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| 4 | nsv1046904 | chr9:96647940-96689327 | Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
| 5 | nsv1035418 | chr9:96647940-96711409 | Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
| 6 | esv1801607 | chr9:96657324-96683214 | Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
| 7 | nsv1042043 | chr9:96657324-96689327 | Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
