Variant report
| Variant | rs1371286 |
|---|---|
| Chromosome Location | chr1:213663144-213663145 |
| allele | C/G |
| 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 |
|---|---|
| ENSG00000225233 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:18)
| rs_ID | r2[population] |
|---|---|
| rs105959 | 0.90[EUR][1000 genomes] |
| rs10864047 | 0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs10864048 | 0.82[EUR][1000 genomes] |
| rs11120139 | 0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs11120146 | 0.82[EUR][1000 genomes] |
| rs11120147 | 0.82[EUR][1000 genomes] |
| rs12128616 | 0.84[EUR][1000 genomes] |
| rs12746075 | 0.82[EUR][1000 genomes] |
| rs1371290 | 0.82[EUR][1000 genomes] |
| rs1566357 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs1566358 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2165130 | 0.82[EUR][1000 genomes] |
| rs2165133 | 0.82[EUR][1000 genomes] |
| rs2173482 | 0.82[EUR][1000 genomes] |
| rs320374 | 0.83[EUR][1000 genomes] |
| rs451083 | 0.83[EUR][1000 genomes] |
| rs4655427 | 0.98[ASN][1000 genomes] |
| rs6666298 | 0.96[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv832525 | chr1:213580476-213782815 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| 2 | nsv549179 | chr1:213641943-213674732 | Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
