Variant report
Variant | rs7091078 |
---|---|
Chromosome Location | chr10:45670937-45670938 |
allele | C/T |
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] |
---|---|
rs11239389 | 1.00[AFR][1000 genomes] |
rs17157448 | 1.00[AMR][1000 genomes] |
rs58720456 | 1.00[AMR][1000 genomes] |
rs59116619 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60354481 | 1.00[AMR][1000 genomes] |
rs7072240 | 1.00[AMR][1000 genomes] |
rs73275136 | 1.00[AMR][1000 genomes] |
rs73275149 | 1.00[AMR][1000 genomes] |
rs73275179 | 1.00[AMR][1000 genomes] |
rs73275183 | 1.00[AMR][1000 genomes] |
rs73277360 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73277362 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73287567 | 1.00[AMR][1000 genomes] |
rs73287569 | 1.00[AMR][1000 genomes] |
rs73287573 | 1.00[AMR][1000 genomes] |
rs73287578 | 1.00[AMR][1000 genomes] |
rs73287579 | 1.00[AMR][1000 genomes] |
rs73287582 | 1.00[AMR][1000 genomes] |
rs73287584 | 1.00[AMR][1000 genomes] |
rs73287589 | 1.00[AMR][1000 genomes] |
rs73287599 | 1.00[AMR][1000 genomes] |
rs73287601 | 1.00[AMR][1000 genomes] |
rs73289603 | 1.00[AMR][1000 genomes] |
rs73289605 | 1.00[AMR][1000 genomes] |
rs73289609 | 1.00[AMR][1000 genomes] |
rs73289610 | 1.00[AMR][1000 genomes] |
rs73289682 | 1.00[AMR][1000 genomes] |
rs73289688 | 1.00[AMR][1000 genomes] |
rs73289692 | 1.00[AMR][1000 genomes] |
rs73289694 | 1.00[AMR][1000 genomes] |
rs73289697 | 1.00[AMR][1000 genomes] |
rs73291604 | 1.00[AMR][1000 genomes] |
rs73291615 | 1.00[AMR][1000 genomes] |
rs73291688 | 1.00[AMR][1000 genomes] |
rs73291689 | 1.00[AMR][1000 genomes] |
rs7902733 | 1.00[AMR][1000 genomes] |
rs7906497 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2750897 | chr10:45550145-45820136 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
2 | nsv895104 | chr10:45636867-45715369 | Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 9 gene(s) | inside rSNPs | diseases |
3 | 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 |
4 | nsv982848 | chr10:45657182-45673875 | Weak transcription Enhancers Flanking Active TSS | TF binding regionChromatin interactive regionlncRNAmiRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv895106 | chr10:45659032-45715369 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
6 | 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 |
7 | nsv947906 | chr10:45669900-45671966 | Enhancers Flanking Active TSS Weak transcription | lncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:45668600-45671200 | Weak transcription | Fetal Heart | heart |
2 | chr10:45670800-45671200 | Flanking Active TSS | K562 | blood |
3 | chr10:45670800-45671600 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr10:45670800-45671600 | Enhancers | Placenta | Placenta |