Variant report
Variant | rs59615645 |
---|---|
Chromosome Location | chr8:64996813-64996814 |
allele | G/T |
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] |
---|---|
rs56686729 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60185055 | 1.00[AMR][1000 genomes] |
rs61083487 | 1.00[AMR][1000 genomes] |
rs61119787 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs61599569 | 1.00[AMR][1000 genomes] |
rs73244044 | 1.00[AMR][1000 genomes] |
rs73244048 | 1.00[AMR][1000 genomes] |
rs73244058 | 1.00[AMR][1000 genomes] |
rs73244518 | 1.00[AMR][1000 genomes] |
rs73244547 | 1.00[AMR][1000 genomes] |
rs73244563 | 1.00[AMR][1000 genomes] |
rs73244569 | 1.00[AMR][1000 genomes] |
rs73244588 | 1.00[AMR][1000 genomes] |
rs73244595 | 1.00[AMR][1000 genomes] |
rs73244597 | 1.00[AMR][1000 genomes] |
rs73246219 | 1.00[AMR][1000 genomes] |
rs73246221 | 1.00[AMR][1000 genomes] |
rs73246230 | 1.00[AMR][1000 genomes] |
rs73246241 | 1.00[AMR][1000 genomes] |
rs73246243 | 1.00[AMR][1000 genomes] |
rs73246246 | 1.00[AMR][1000 genomes] |
rs73246249 | 1.00[AMR][1000 genomes] |
rs73246251 | 1.00[AMR][1000 genomes] |
rs73246253 | 1.00[AMR][1000 genomes] |
rs7830204 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948343 | chr8:64804219-65328394 | Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv890969 | chr8:64807144-65047353 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv890970 | chr8:64975466-65125295 | ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
4 | nsv534001 | chr8:64992196-65798776 | Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 17 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:64993000-65004800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |