Variant report
Variant | rs6079804 |
---|---|
Chromosome Location | chr20:15389244-15389245 |
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] |
---|---|
rs11698317 | 0.82[YRI][hapmap] |
rs17678835 | 0.82[YRI][hapmap] |
rs389269 | 0.90[CHB][hapmap] |
rs433078 | 0.90[CHB][hapmap] |
rs4814367 | 0.80[AMR][1000 genomes] |
rs4814368 | 0.90[CHB][hapmap] |
rs4814369 | 0.90[CHB][hapmap] |
rs4814372 | 0.90[CHB][hapmap] |
rs6034182 | 0.90[CHB][hapmap] |
rs6034187 | 0.90[CHB][hapmap] |
rs6043270 | 0.80[CHB][hapmap] |
rs6043273 | 0.89[CHB][hapmap] |
rs6074888 | 0.89[CHB][hapmap] |
rs6074891 | 0.90[CHB][hapmap];1.00[YRI][hapmap] |
rs6079806 | 1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6079807 | 0.90[CHB][hapmap] |
rs6079808 | 0.90[CHB][hapmap] |
rs6079809 | 0.89[CHB][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes] |
rs6079810 | 0.90[CHB][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes] |
rs6079811 | 0.90[CHB][hapmap];0.87[AMR][1000 genomes] |
rs6079816 | 0.90[CHB][hapmap] |
rs6079819 | 0.90[CHB][hapmap] |
rs6079822 | 0.90[CHB][hapmap] |
rs888205 | 0.90[CHB][hapmap] |
rs927919 | 0.90[CHB][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes] |
rs932823 | 0.80[CHB][hapmap] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1062252 | chr20:14964258-15547739 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv544206 | chr20:14964258-15547739 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv869328 | chr20:15325423-16213898 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv833927 | chr20:15362602-15520185 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:15388800-15389600 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |