Variant report
| Variant | rs66691946 |
|---|---|
| Chromosome Location | chr2:174142528-174142529 |
| allele | C/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:
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| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000238133 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:10)
| rs_ID | r2[population] |
|---|---|
| rs11685378 | 0.90[AMR][1000 genomes];0.83[ASN][1000 genomes] |
| rs11692098 | 0.90[AMR][1000 genomes];0.88[ASN][1000 genomes] |
| rs11695778 | 0.88[ASN][1000 genomes] |
| rs12618933 | 0.90[AMR][1000 genomes];0.82[ASN][1000 genomes] |
| rs12620774 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs13023958 | 0.90[AMR][1000 genomes];0.84[ASN][1000 genomes] |
| rs13031154 | 0.86[ASN][1000 genomes] |
| rs3769148 | 0.89[AMR][1000 genomes];0.84[ASN][1000 genomes] |
| rs66483031 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes] |
| rs752077 | 0.90[AMR][1000 genomes];0.85[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1011724 | chr2:173916482-174231908 | Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
