Variant report
Variant | rs6471996 |
---|---|
Chromosome Location | chr8:63023132-63023133 |
allele | A/C |
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] |
---|---|
rs10092163 | 0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10096181 | 0.94[ASN][1000 genomes] |
rs4348484 | 0.94[CEU][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4352846 | 0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6471994 | 0.88[CEU][hapmap] |
rs6471995 | 0.88[CEU][hapmap] |
rs7818020 | 0.87[CEU][hapmap] |
rs7818029 | 0.86[CEU][hapmap] |
rs7834120 | 0.92[CEU][hapmap];1.00[CHB][hapmap] |
rs7834643 | 0.88[CEU][hapmap] |
rs978253 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv890954 | chr8:62919691-63023132 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv890955 | chr8:62919691-63062581 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1032321 | chr8:62954064-63026567 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |