Variant report
Variant | rs6884332 |
---|---|
Chromosome Location | chr5:108570321-108570322 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11743213 | 0.85[EUR][1000 genomes] |
rs12515174 | 0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12520021 | 0.86[ASN][1000 genomes] |
rs12522058 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12522411 | 0.86[ASN][1000 genomes] |
rs1363214 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1422003 | 0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs17473588 | 0.95[AFR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs17473831 | 0.86[EUR][1000 genomes] |
rs4346815 | 0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4645374 | 0.86[ASN][1000 genomes] |
rs57400924 | 0.84[AFR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs60496657 | 0.86[ASN][1000 genomes] |
rs62376831 | 0.86[EUR][1000 genomes] |
rs62376832 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6864796 | 0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6866668 | 0.86[ASN][1000 genomes] |
rs6877495 | 0.86[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6881141 | 0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6899020 | 0.86[ASN][1000 genomes] |
rs7700949 | 0.86[ASN][1000 genomes] |
rs7715416 | 0.83[ASN][1000 genomes] |
rs7718897 | 0.85[ASN][1000 genomes] |
rs7720237 | 0.86[ASN][1000 genomes] |
rs7727900 | 0.95[AFR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9968753 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1027163 | chr5:108445447-108839913 | Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
2 | nsv599338 | chr5:108528729-108675737 | Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:108570200-108570400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |