Variant report
Variant | rs2676632 |
---|---|
Chromosome Location | chr8:69335234-69335235 |
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] |
---|---|
rs1517129 | 0.93[EUR][1000 genomes] |
rs17467559 | 0.95[EUR][1000 genomes] |
rs2243700 | 0.97[EUR][1000 genomes] |
rs2243702 | 0.97[EUR][1000 genomes] |
rs2246592 | 1.00[EUR][1000 genomes] |
rs2255882 | 0.96[EUR][1000 genomes] |
rs2591010 | 0.98[EUR][1000 genomes] |
rs2591014 | 0.98[EUR][1000 genomes] |
rs2591019 | 0.93[EUR][1000 genomes] |
rs2591020 | 0.93[EUR][1000 genomes] |
rs2591021 | 0.94[EUR][1000 genomes] |
rs2591024 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2676649 | 0.93[EUR][1000 genomes] |
rs2676650 | 0.86[EUR][1000 genomes] |
rs2676651 | 0.94[EUR][1000 genomes] |
rs2676653 | 0.94[EUR][1000 genomes] |
rs2676654 | 0.96[EUR][1000 genomes] |
rs2676655 | 0.97[EUR][1000 genomes] |
rs2676656 | 0.96[EUR][1000 genomes] |
rs814442 | 0.81[EUR][1000 genomes] |
rs814455 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948687 | chr8:69041121-69642540 | Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1023810 | chr8:69308665-69440129 | Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv539644 | chr8:69308665-69440129 | Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv820237 | chr8:69327804-69344263 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:69317200-69342600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |