Variant report
| Variant | rs7132837 |
|---|---|
| Chromosome Location | chr12:124282761-124282762 |
| allele | A/G |
| 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 |
| rs_ID | r2[population] |
|---|---|
| rs1050443 | 1.00[CHD][hapmap] |
| rs1050448 | 1.00[CHD][hapmap] |
| rs12579670 | 1.00[TSI][hapmap] |
| rs12580578 | 1.00[TSI][hapmap] |
| rs12581508 | 1.00[TSI][hapmap] |
| rs3204541 | 1.00[CHD][hapmap] |
| rs7969937 | 1.00[TSI][hapmap] |
| rs7977449 | 1.00[TSI][hapmap] |
| rs7980049 | 1.00[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 | nsv498024 | chr12:123994372-124459856 | Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 63 gene(s) | inside rSNPs | diseases |
| No data |





