Variant report
Variant | rs315968 |
---|---|
Chromosome Location | chr8:87709335-87709336 |
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] |
---|---|
rs12155947 | 0.93[CEU][hapmap] |
rs1372171 | 0.93[CEU][hapmap] |
rs1372172 | 0.93[CEU][hapmap] |
rs1372173 | 0.93[CEU][hapmap];1.00[GIH][hapmap];0.89[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap] |
rs1441241 | 0.93[CEU][hapmap] |
rs1441242 | 0.93[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap] |
rs188808 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs315959 | 1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs315961 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs315970 | 1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs315971 | 1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs315975 | 1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4960986 | 0.93[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes] |
rs6471449 | 0.84[EUR][1000 genomes] |
rs6471476 | 0.93[CEU][hapmap] |
rs6471482 | 0.93[CEU][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap] |
rs6997641 | 0.93[CEU][hapmap] |
rs766451 | 0.93[CEU][hapmap] |
rs7812988 | 0.93[CEU][hapmap] |
rs9297946 | 0.93[CEU][hapmap] |
rs970633 | 0.93[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1023510 | chr8:87429001-87874948 | Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
2 | nsv891151 | chr8:87690019-87776019 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv1026794 | chr8:87698639-87957840 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv539662 | chr8:87698639-87957840 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |