Variant report
Variant | rs954416 |
---|---|
Chromosome Location | chr4:81760308-81760309 |
allele | A/G |
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] |
---|---|
rs1027294 | 0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs1027295 | 1.00[JPT][hapmap] |
rs10516649 | 0.88[CHB][hapmap];1.00[JPT][hapmap] |
rs11099448 | 0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs12233641 | 0.93[ASN][1000 genomes] |
rs12233814 | 0.93[ASN][1000 genomes] |
rs12648780 | 0.98[ASN][1000 genomes] |
rs12648781 | 0.98[ASN][1000 genomes] |
rs13102852 | 0.93[ASN][1000 genomes] |
rs13108385 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13119650 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs13129485 | 1.00[JPT][hapmap] |
rs34269465 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34620960 | 0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs35093266 | 0.83[EUR][1000 genomes] |
rs35227775 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs35336312 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35443534 | 0.93[ASN][1000 genomes] |
rs35663002 | 0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs36002245 | 0.93[ASN][1000 genomes] |
rs36087364 | 0.82[ASN][1000 genomes] |
rs71596035 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1002776 | chr4:81480374-81802614 | Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv537154 | chr4:81480374-81802614 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | esv3518601 | chr4:81523238-81831941 | Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv3518602 | chr4:81523354-81831976 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:81753400-81761800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |