Variant report
Variant | rs2886581 |
---|---|
Chromosome Location | chr14:78866661-78866662 |
allele | A/C |
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] |
---|---|
rs10135111 | 1.00[AMR][1000 genomes] |
rs10135475 | 1.00[AMR][1000 genomes] |
rs11159360 | 1.00[AMR][1000 genomes] |
rs1156946 | 1.00[AMR][1000 genomes] |
rs1990530 | 1.00[AMR][1000 genomes] |
rs2052202 | 1.00[AMR][1000 genomes] |
rs2052203 | 1.00[AMR][1000 genomes] |
rs2110424 | 1.00[AMR][1000 genomes] |
rs2192413 | 1.00[AMR][1000 genomes] |
rs2192414 | 1.00[AMR][1000 genomes] |
rs2192415 | 1.00[AMR][1000 genomes] |
rs2192421 | 1.00[AMR][1000 genomes] |
rs2215830 | 1.00[AMR][1000 genomes] |
rs2215831 | 1.00[AMR][1000 genomes] |
rs2215832 | 1.00[AMR][1000 genomes] |
rs2215833 | 1.00[AMR][1000 genomes] |
rs2366099 | 1.00[AMR][1000 genomes] |
rs2366156 | 1.00[AMR][1000 genomes] |
rs4899709 | 1.00[AMR][1000 genomes] |
rs4899710 | 1.00[AMR][1000 genomes] |
rs4903756 | 1.00[AMR][1000 genomes] |
rs4903765 | 1.00[AMR][1000 genomes] |
rs6574444 | 1.00[AMR][1000 genomes] |
rs6574449 | 1.00[AMR][1000 genomes] |
rs6574450 | 1.00[AMR][1000 genomes] |
rs7157498 | 1.00[AMR][1000 genomes] |
rs7158579 | 1.00[AMR][1000 genomes] |
rs7159492 | 1.00[AMR][1000 genomes] |
rs8003367 | 1.00[AMR][1000 genomes] |
rs8003391 | 1.00[AMR][1000 genomes] |
rs8005882 | 1.00[AMR][1000 genomes] |
rs8008949 | 1.00[AMR][1000 genomes] |
rs8017182 | 1.00[AMR][1000 genomes] |
rs8020682 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832837 | chr14:78766805-78946526 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:78865200-78869400 | Weak transcription | Brain Angular Gyrus | brain |
2 | chr14:78865400-78871200 | Weak transcription | Brain Anterior Caudate | brain |