Variant report
Variant | rs16907514 |
---|---|
Chromosome Location | chr12:12061226-12061227 |
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] |
---|---|
rs55977745 | 1.00[AMR][1000 genomes] |
rs56140733 | 1.00[AMR][1000 genomes] |
rs57312986 | 1.00[AMR][1000 genomes] |
rs57699137 | 1.00[AMR][1000 genomes] |
rs57833941 | 1.00[AMR][1000 genomes] |
rs57891658 | 1.00[AMR][1000 genomes] |
rs58453187 | 1.00[AMR][1000 genomes] |
rs58842201 | 1.00[AMR][1000 genomes] |
rs59632980 | 1.00[AMR][1000 genomes] |
rs59843195 | 1.00[AMR][1000 genomes] |
rs73275248 | 1.00[AMR][1000 genomes] |
rs73290521 | 1.00[AMR][1000 genomes] |
rs73290524 | 1.00[AMR][1000 genomes] |
rs73290599 | 1.00[AMR][1000 genomes] |
rs74060863 | 1.00[AMR][1000 genomes] |
rs74060864 | 1.00[AMR][1000 genomes] |
rs74060865 | 1.00[AMR][1000 genomes] |
rs74060867 | 1.00[AMR][1000 genomes] |
rs74060875 | 1.00[AMR][1000 genomes] |
rs74060876 | 1.00[AMR][1000 genomes] |
rs74060879 | 1.00[AMR][1000 genomes] |
rs74060881 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832331 | chr12:11925095-12114451 | Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
2 | nsv949003 | chr12:11938229-12618690 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 36 gene(s) | inside rSNPs | diseases |
3 | nsv898804 | chr12:12058411-12202173 | Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:12060600-12062600 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |