Variant report
Variant | rs17104136 |
---|---|
Chromosome Location | chr12:68004728-68004729 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000127334 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1731770 | 1.00[AMR][1000 genomes] |
rs2700056 | 1.00[AMR][1000 genomes] |
rs2700061 | 1.00[AMR][1000 genomes] |
rs2700063 | 1.00[AMR][1000 genomes] |
rs35314758 | 1.00[AMR][1000 genomes] |
rs6581762 | 1.00[AMR][1000 genomes] |
rs7956219 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3430007 | chr12:67947726-68241938 | Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No data |