Variant report
Variant | rs1905846 |
---|---|
Chromosome Location | chr3:84658657-84658658 |
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] |
---|---|
rs12488651 | 0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1473461 | 0.91[ASN][1000 genomes] |
rs1580448 | 0.91[ASN][1000 genomes] |
rs17492563 | 0.90[ASN][1000 genomes] |
rs17500476 | 0.84[ASN][1000 genomes] |
rs56985130 | 0.91[ASN][1000 genomes] |
rs59551717 | 0.86[ASN][1000 genomes] |
rs59671531 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs62254217 | 0.98[ASN][1000 genomes] |
rs62254685 | 0.87[ASN][1000 genomes] |
rs62254689 | 0.87[ASN][1000 genomes] |
rs62254714 | 0.91[ASN][1000 genomes] |
rs62254715 | 0.91[ASN][1000 genomes] |
rs6781297 | 0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6782948 | 0.92[ASN][1000 genomes] |
rs72907319 | 0.83[EUR][1000 genomes] |
rs72907321 | 0.83[EUR][1000 genomes] |
rs73127115 | 0.91[ASN][1000 genomes] |
rs9309944 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs974534 | 0.94[ASN][1000 genomes] |
rs974535 | 0.98[ASN][1000 genomes] |
rs9837600 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9839147 | 0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2760745 | chr3:84208364-84783259 | Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv998578 | chr3:84521514-84773582 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv536615 | chr3:84521514-84773582 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv460745 | chr3:84644186-84779079 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
5 | nsv590851 | chr3:84644186-84779079 | Enhancers Flanking Active TSS Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
6 | nsv1014928 | chr3:84653836-84773582 | Enhancers Active TSS Weak transcription Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
7 | nsv536616 | chr3:84653836-84773582 | Active TSS Enhancers Weak transcription Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:84658400-84659600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |