Variant report
Variant | rs59351220 |
---|---|
Chromosome Location | chr8:34806779-34806780 |
allele | C/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] |
---|---|
rs10095892 | 1.00[ASN][1000 genomes] |
rs10100037 | 1.00[ASN][1000 genomes] |
rs10100826 | 1.00[ASN][1000 genomes] |
rs10102708 | 0.83[AFR][1000 genomes] |
rs10103055 | 1.00[ASN][1000 genomes] |
rs10103980 | 1.00[ASN][1000 genomes] |
rs10105808 | 0.89[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10112862 | 1.00[ASN][1000 genomes] |
rs10112892 | 1.00[ASN][1000 genomes] |
rs10113755 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11985082 | 1.00[ASN][1000 genomes] |
rs11985509 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11996585 | 0.89[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13439316 | 1.00[ASN][1000 genomes] |
rs16883296 | 1.00[ASN][1000 genomes] |
rs16883314 | 1.00[ASN][1000 genomes] |
rs16883318 | 1.00[ASN][1000 genomes] |
rs16883376 | 1.00[ASN][1000 genomes] |
rs28665220 | 0.86[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28722910 | 1.00[ASN][1000 genomes] |
rs4428666 | 1.00[ASN][1000 genomes] |
rs67632002 | 1.00[ASN][1000 genomes] |
rs6995753 | 1.00[ASN][1000 genomes] |
rs7017513 | 1.00[ASN][1000 genomes] |
rs72629548 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72631003 | 1.00[ASN][1000 genomes] |
rs7817114 | 1.00[ASN][1000 genomes] |
rs7839246 | 1.00[ASN][1000 genomes] |
rs7840788 | 1.00[ASN][1000 genomes] |
rs7843585 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv890716 | chr8:34707436-34822797 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
2 | nsv1017085 | chr8:34742896-35594241 | Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv539546 | chr8:34742896-35594241 | Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:34804400-34808200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr8:34804800-34808200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |