Variant report
Variant | rs6772636 |
---|---|
Chromosome Location | chr3:180366870-180366871 |
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 |
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000242808 | Chromatin interaction |
ENSG00000205981 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs3860513 | 0.86[CEU][hapmap] |
rs58906660 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs61111878 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6766929 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6769457 | 0.81[CEU][hapmap];0.85[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9846084 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs9869523 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3359190 | chr3:180298396-180397223 | Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv999338 | chr3:180348143-181160251 | Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 41 gene(s) | inside rSNPs | diseases |
No data |