Variant report
Variant | rs9493242 |
---|---|
Chromosome Location | chr6:132543445-132543446 |
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 |
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Variant related genes | Relation type |
---|---|
ENSG00000118523 | Chromatin interaction |
ENSG00000227220 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs9483416 | 1.00[AFR][1000 genomes] |
rs9483424 | 0.83[AFR][1000 genomes] |
rs9493245 | 1.00[AFR][1000 genomes] |
rs9493246 | 1.00[AFR][1000 genomes] |
rs9493260 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2762616 | chr6:132404708-132584324 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 22 gene(s) | inside rSNPs | diseases |
2 | nsv1024527 | chr6:132532941-132571889 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |