Variant report
| Variant | rs3803208 |
|---|---|
| Chromosome Location | chr13:92902492-92902493 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:22)
| rs_ID | r2[population] |
|---|---|
| rs11842003 | 1.00[JPT][hapmap] |
| rs1360390 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs1360391 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs1360392 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs1360393 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs2148523 | 1.00[JPT][hapmap] |
| rs7333645 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs7335555 | 1.00[JPT][hapmap] |
| rs7981670 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs7991537 | 1.00[JPT][hapmap] |
| rs7995221 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs9301783 | 1.00[JPT][hapmap] |
| rs9560960 | 1.00[JPT][hapmap] |
| rs9560961 | 1.00[JPT][hapmap] |
| rs9560972 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs9560973 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs9560974 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs9560977 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
| rs9560981 | 1.00[JPT][hapmap] |
| rs9560995 | 1.00[JPT][hapmap] |
| rs9560997 | 1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs9583999 | 1.00[JPT][hapmap] |
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 | esv2756005 | chr13:92584199-93080799 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
| 2 | nsv1035365 | chr13:92805325-92926114 | Enhancers Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
| 3 | nsv456067 | chr13:92868073-92967664 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 4 | nsv562726 | chr13:92868073-92967664 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 5 | nsv900902 | chr13:92884370-92942274 | Weak transcription Enhancers Active TSS | n/a | n/a | inside rSNPs | diseases |
| 6 | nsv527287 | chr13:92901926-92911496 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
| 7 | nsv983763 | chr13:92902437-92906021 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:92902400-92902800 | Enhancers | Fetal Stomach | stomach |
