Variant report
Variant | rs1168588 |
---|---|
Chromosome Location | chr10:27926210-27926211 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:27926074..27926787-chr10:28009084..28009786,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1168571 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1168572 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1168574 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1168582 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1168583 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1168585 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1168586 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1168589 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1631705 | 0.95[AFR][1000 genomes] |
rs1687722 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1687723 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1687724 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1687730 | 0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1687731 | 0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1687732 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1687733 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1687735 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1687736 | 0.87[EUR][1000 genomes] |
rs1690678 | 0.92[EUR][1000 genomes] |
rs1690684 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1690685 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1690686 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2453213 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2491324 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2505134 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2815539 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv550241 | chr10:27569521-28025771 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
2 | nsv1045257 | chr10:27572440-27926946 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
3 | esv3368825 | chr10:27864181-28043820 | Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
4 | nsv894985 | chr10:27869503-27957785 | Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv894986 | chr10:27904646-27957785 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:27926000-27927400 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
2 | chr10:27926200-27927800 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |