Variant report
Variant | rs9822411 |
---|---|
Chromosome Location | chr3:25363943-25363944 |
allele | A/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] |
---|---|
rs11707139 | 0.87[EUR][1000 genomes] |
rs11709623 | 0.87[EUR][1000 genomes] |
rs11709732 | 0.90[EUR][1000 genomes] |
rs11714481 | 0.87[EUR][1000 genomes] |
rs11716065 | 0.87[EUR][1000 genomes] |
rs11717848 | 0.90[EUR][1000 genomes] |
rs11718046 | 0.90[EUR][1000 genomes] |
rs11718836 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs11720675 | 0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs11721271 | 0.90[EUR][1000 genomes] |
rs17016187 | 0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs17016204 | 0.83[ASN][1000 genomes] |
rs17016260 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs17588596 | 0.86[CEU][hapmap];0.88[JPT][hapmap];0.90[EUR][1000 genomes] |
rs1984597 | 0.83[ASN][1000 genomes] |
rs2164476 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes] |
rs57697446 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs6550962 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs6550963 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs6550966 | 0.90[EUR][1000 genomes] |
rs7615094 | 0.90[EUR][1000 genomes] |
rs7623030 | 0.86[EUR][1000 genomes] |
rs7649070 | 0.87[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs9818293 | 0.83[ASN][1000 genomes] |
rs9837851 | 0.83[ASN][1000 genomes] |
rs9877461 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949035 | chr3:25194301-26084890 | Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 68 gene(s) | inside rSNPs | diseases |
2 | nsv876632 | chr3:25325479-25366205 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv834645 | chr3:25363723-25555107 | Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |