Variant report
Variant | rs16899679 |
---|---|
Chromosome Location | chr5:29887070-29887071 |
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] |
---|---|
rs10520953 | 0.91[CEU][hapmap];0.83[CHB][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap] |
rs12697227 | 0.83[CHB][hapmap];0.86[MEX][hapmap] |
rs1428318 | 0.97[EUR][1000 genomes] |
rs1428321 | 0.91[CEU][hapmap];0.83[CHB][hapmap];0.97[EUR][1000 genomes] |
rs16899550 | 0.82[CHB][hapmap];0.97[EUR][1000 genomes] |
rs16899578 | 0.82[CHB][hapmap] |
rs16899668 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs72745276 | 0.97[EUR][1000 genomes] |
rs72745277 | 0.97[EUR][1000 genomes] |
rs72745278 | 0.95[EUR][1000 genomes] |
rs72745295 | 0.97[EUR][1000 genomes] |
rs9292344 | 0.97[EUR][1000 genomes] |
rs9790891 | 0.97[EUR][1000 genomes] |
rs9791032 | 0.97[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3385368 | chr5:29548608-29910057 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv1018779 | chr5:29861138-29937229 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1029641 | chr5:29861138-29940871 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2763448 | chr5:29875965-29887070 | Inactive region | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
No data |