Variant report
Variant | rs59303804 |
---|---|
Chromosome Location | chr3:80798540-80798541 |
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 |
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rs_ID | r2[population] |
---|---|
rs10049368 | 1.00[AMR][1000 genomes] |
rs17018281 | 0.98[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs56059271 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs56091124 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs56198464 | 0.92[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs56802446 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57189276 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57211378 | 1.00[AMR][1000 genomes] |
rs57495637 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59448649 | 0.92[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs61598826 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6764754 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6800151 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73851790 | 0.85[AMR][1000 genomes] |
rs73852203 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73854221 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73854222 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73854230 | 0.92[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs73854233 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73854234 | 0.95[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs73854942 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7614247 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7624579 | 1.00[AMR][1000 genomes] |
rs7625164 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9682002 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9843591 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1004115 | chr3:80349665-81043308 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv536601 | chr3:80349665-81043308 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
3 | nsv1067580 | chr3:80416729-81043307 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
4 | nsv492220 | chr3:80416729-81043307 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
5 | nsv1000592 | chr3:80422155-81044175 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
6 | nsv527598 | chr3:80585455-81250663 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
7 | nsv877037 | chr3:80611818-80811252 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | nsv877038 | chr3:80781726-80984958 | Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
9 | esv1846627 | chr3:80791380-80912454 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:80796400-80801600 | Weak transcription | Brain Germinal Matrix | brain |
2 | chr3:80796400-80801800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
3 | chr3:80796400-80802200 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |