Variant report
| Variant | rs73092441 |
|---|---|
| Chromosome Location | chr12:33081766-33081767 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr12:33048729..33051002-chr12:33080642..33082544,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000057294 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:27)
| rs_ID | r2[population] |
|---|---|
| rs11837196 | 1.00[AMR][1000 genomes] |
| rs11837863 | 1.00[AMR][1000 genomes] |
| rs4076730 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs57076983 | 1.00[AMR][1000 genomes] |
| rs58326642 | 1.00[AMR][1000 genomes] |
| rs73092447 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73092461 | 1.00[EUR][1000 genomes] |
| rs73092462 | 1.00[EUR][1000 genomes] |
| rs73092464 | 1.00[EUR][1000 genomes] |
| rs73092465 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73092467 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73092469 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73092471 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73092477 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73092481 | 1.00[EUR][1000 genomes] |
| rs73092701 | 1.00[AMR][1000 genomes] |
| rs73094516 | 1.00[AMR][1000 genomes] |
| rs73094523 | 1.00[AMR][1000 genomes] |
| rs73094525 | 1.00[AMR][1000 genomes] |
| rs73094527 | 1.00[AMR][1000 genomes] |
| rs73094584 | 1.00[AMR][1000 genomes] |
| rs73094587 | 1.00[AMR][1000 genomes] |
| rs73096635 | 1.00[AMR][1000 genomes] |
| rs73096690 | 1.00[AMR][1000 genomes] |
| rs73098610 | 1.00[AMR][1000 genomes] |
| rs73098627 | 1.00[AMR][1000 genomes] |
| rs73098635 | 1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv530421 | chr12:32825335-33465991 | Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
| 2 | nsv1054440 | chr12:32872999-33150460 | Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
| 3 | nsv832367 | chr12:33063644-33298967 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:33080800-33082000 | Weak transcription | Placenta | Placenta |
