Variant report
Variant | rs10111178 |
---|---|
Chromosome Location | chr8:10825941-10825942 |
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] |
---|---|
rs10086778 | 1.00[JPT][hapmap] |
rs10086872 | 1.00[JPT][hapmap] |
rs10087882 | 0.87[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10094007 | 1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10094337 | 1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10094684 | 1.00[JPT][hapmap] |
rs10095039 | 1.00[JPT][hapmap] |
rs10095261 | 1.00[JPT][hapmap] |
rs10095390 | 1.00[JPT][hapmap] |
rs10096624 | 1.00[JPT][hapmap] |
rs10096634 | 1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10096872 | 1.00[JPT][hapmap] |
rs10097626 | 1.00[JPT][hapmap] |
rs10098549 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes] |
rs10102369 | 0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10106574 | 1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10107105 | 0.81[EUR][1000 genomes] |
rs10107544 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes] |
rs10107658 | 1.00[JPT][hapmap] |
rs10112255 | 1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10903334 | 0.88[AMR][1000 genomes] |
rs11250100 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11985330 | 1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11990141 | 0.88[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs11995188 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28546463 | 0.83[AMR][1000 genomes] |
rs28712086 | 0.83[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs4265148 | 1.00[JPT][hapmap] |
rs4314618 | 1.00[JPT][hapmap] |
rs4434585 | 1.00[JPT][hapmap] |
rs4623374 | 1.00[JPT][hapmap] |
rs4626559 | 1.00[JPT][hapmap] |
rs4645525 | 1.00[JPT][hapmap] |
rs57698321 | 0.88[AMR][1000 genomes] |
rs6601540 | 1.00[JPT][hapmap] |
rs6982927 | 1.00[JPT][hapmap] |
rs7008460 | 1.00[JPT][hapmap] |
rs73537380 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7816172 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv917085 | chr8:10237508-10828204 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
2 | nsv521721 | chr8:10802102-10836472 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv1035072 | chr8:10819444-11480692 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
4 | nsv539473 | chr8:10819444-11480692 | Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:10824400-10826000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr8:10824600-10829200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr8:10825800-10826200 | Bivalent Enhancer | Fetal Muscle Trunk | muscle |
4 | chr8:10825800-10827200 | Enhancers | Fetal Muscle Leg | muscle |