Variant report
Variant | rs6887436 |
---|---|
Chromosome Location | chr5:116513359-116513360 |
allele | C/T |
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] |
---|---|
rs10037464 | 0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10069214 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11241418 | 0.86[ASN][1000 genomes] |
rs11949654 | 0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11956143 | 0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13178735 | 1.00[ASN][1000 genomes] |
rs28509225 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs6595013 | 0.90[ASN][1000 genomes] |
rs6595014 | 0.90[ASN][1000 genomes] |
rs6595017 | 0.83[ASN][1000 genomes] |
rs6868320 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6886341 | 0.90[ASN][1000 genomes] |
rs6887392 | 1.00[ASN][1000 genomes] |
rs6887868 | 1.00[ASN][1000 genomes] |
rs6891915 | 0.90[ASN][1000 genomes] |
rs6892201 | 0.90[ASN][1000 genomes] |
rs6897500 | 0.90[ASN][1000 genomes] |
rs7704021 | 0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7715599 | 0.90[ASN][1000 genomes] |
rs7731335 | 0.83[ASN][1000 genomes] |
rs9327035 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv882752 | chr5:116505127-116549323 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | n/a | n/a | inside rSNPs | n/a |
2 | nsv882753 | chr5:116505127-116549669 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | n/a | n/a | inside rSNPs | n/a |
3 | nsv882754 | chr5:116505127-116553503 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:116512600-116513800 | Enhancers | HepG2 | liver |