Variant report
Variant | rs16914957 |
---|---|
Chromosome Location | chr11:25986830-25986831 |
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] |
---|---|
rs1027139 | 0.86[EUR][1000 genomes] |
rs10501027 | 1.00[ASN][1000 genomes] |
rs11028985 | 1.00[ASN][1000 genomes] |
rs12282542 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12282654 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12364146 | 1.00[ASN][1000 genomes] |
rs12796585 | 1.00[ASN][1000 genomes] |
rs1441511 | 1.00[ASN][1000 genomes] |
rs16914910 | 1.00[ASN][1000 genomes] |
rs17242747 | 1.00[ASN][1000 genomes] |
rs17242753 | 1.00[ASN][1000 genomes] |
rs17242774 | 1.00[ASN][1000 genomes] |
rs17308523 | 1.00[ASN][1000 genomes] |
rs17308621 | 1.00[ASN][1000 genomes] |
rs1901416 | 1.00[ASN][1000 genomes] |
rs6484186 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67141149 | 1.00[ASN][1000 genomes] |
rs67333685 | 1.00[ASN][1000 genomes] |
rs7106427 | 1.00[ASN][1000 genomes] |
rs7123239 | 1.00[ASN][1000 genomes] |
rs72872807 | 0.87[ASN][1000 genomes] |
rs72872842 | 1.00[ASN][1000 genomes] |
rs72875022 | 1.00[ASN][1000 genomes] |
rs72875027 | 1.00[ASN][1000 genomes] |
rs72875031 | 1.00[ASN][1000 genomes] |
rs72875080 | 1.00[ASN][1000 genomes] |
rs72875083 | 0.86[EUR][1000 genomes] |
rs72875094 | 1.00[ASN][1000 genomes] |
rs72876806 | 1.00[ASN][1000 genomes] |
rs72876822 | 0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72876823 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72876824 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72876833 | 0.82[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs7932544 | 1.00[ASN][1000 genomes] |
rs7936563 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7937836 | 1.00[ASN][1000 genomes] |
rs973832 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2760599 | chr11:25186984-26159450 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv1046507 | chr11:25469712-26111707 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv832091 | chr11:25823826-26009887 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv469948 | chr11:25859783-26026233 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1041778 | chr11:25898574-26098141 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv897140 | chr11:25905509-25991194 | Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:25974400-25989400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr11:25979400-25988600 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |