Variant report
Variant | rs16914386 |
---|---|
Chromosome Location | chr8:51086359-51086360 |
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 |
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No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10086701 | 1.00[AMR][1000 genomes] |
rs10086711 | 1.00[AMR][1000 genomes] |
rs10087717 | 1.00[AMR][1000 genomes] |
rs10092855 | 1.00[AMR][1000 genomes] |
rs10095854 | 1.00[AMR][1000 genomes] |
rs10098968 | 1.00[AMR][1000 genomes] |
rs10100178 | 1.00[AMR][1000 genomes] |
rs10102192 | 1.00[AMR][1000 genomes] |
rs10103196 | 1.00[AMR][1000 genomes] |
rs10105597 | 1.00[AMR][1000 genomes] |
rs10105663 | 1.00[AMR][1000 genomes] |
rs10108552 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10110083 | 1.00[AMR][1000 genomes] |
rs10110244 | 1.00[AMR][1000 genomes] |
rs10110791 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11986830 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11995916 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12334688 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16914314 | 1.00[AMR][1000 genomes] |
rs16914324 | 1.00[AMR][1000 genomes] |
rs16914325 | 1.00[AMR][1000 genomes] |
rs16914366 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16914373 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16914384 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16914392 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16914395 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16914462 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28546668 | 1.00[AMR][1000 genomes] |
rs28642790 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28644781 | 1.00[AMR][1000 genomes] |
rs28654110 | 1.00[AMR][1000 genomes] |
rs28760868 | 1.00[AMR][1000 genomes] |
rs28773838 | 1.00[AMR][1000 genomes] |
rs56804531 | 1.00[AMR][1000 genomes] |
rs9987189 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3353749 | chr8:50530807-51139242 | Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv916392 | chr8:50827638-51395140 | Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv2759613 | chr8:50873293-51137995 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2758621 | chr8:50886593-51137995 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | esv1829361 | chr8:51021638-51101126 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv1027984 | chr8:51060895-51098808 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv1022362 | chr8:51071742-51093985 | Enhancers ZNF genes & repeats Weak transcription Strong transcription | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | nsv8340 | chr8:51085564-51087130 | ZNF genes & repeats Weak transcription Enhancers Strong transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:51082600-51086400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
2 | chr8:51085600-51091200 | Weak transcription | Cortex derived primary cultured neurospheres | brain |