Variant report
Variant | rs12360419 |
---|---|
Chromosome Location | chr10:45825659-45825660 |
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] |
---|---|
rs10159580 | 0.81[EUR][1000 genomes] |
rs10793613 | 0.81[EUR][1000 genomes] |
rs10900195 | 0.81[EUR][1000 genomes] |
rs10900200 | 0.81[EUR][1000 genomes] |
rs11239432 | 0.81[EUR][1000 genomes] |
rs11239434 | 0.80[EUR][1000 genomes] |
rs11239435 | 0.81[EUR][1000 genomes] |
rs11239437 | 0.81[EUR][1000 genomes] |
rs11239452 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs11522532 | 0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs11523407 | 0.83[EUR][1000 genomes] |
rs11523866 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12250005 | 0.81[EUR][1000 genomes] |
rs12268890 | 0.81[EUR][1000 genomes] |
rs12355722 | 0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs12357069 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12358110 | 0.81[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs1529828 | 0.81[EUR][1000 genomes] |
rs1529829 | 0.81[EUR][1000 genomes] |
rs17521948 | 0.81[EUR][1000 genomes] |
rs1968475 | 0.82[EUR][1000 genomes] |
rs28485654 | 0.82[AFR][1000 genomes] |
rs28570111 | 0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs28688874 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs55963543 | 0.81[EUR][1000 genomes] |
rs7085353 | 0.81[EUR][1000 genomes] |
rs72786508 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs72788095 | 0.81[EUR][1000 genomes] |
rs72788096 | 0.81[EUR][1000 genomes] |
rs9664826 | 0.80[EUR][1000 genomes] |
rs9733175 | 0.80[EUR][1000 genomes] |
rs9733444 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv895105 | chr10:45636867-45928822 | Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv430166 | chr10:45668894-46148794 | Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
3 | nsv993428 | chr10:45742877-46224333 | Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:45825600-45825800 | Enhancers | K562 | blood |