Variant report
Variant | rs73402619 |
---|---|
Chromosome Location | chr22:30540406-30540407 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs16988115 | 1.00[AMR][1000 genomes] |
rs16988122 | 1.00[AMR][1000 genomes] |
rs16988151 | 1.00[AMR][1000 genomes] |
rs56733052 | 1.00[AMR][1000 genomes] |
rs57724305 | 1.00[AMR][1000 genomes] |
rs58952888 | 0.91[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs59580785 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs5997565 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6006309 | 1.00[AMR][1000 genomes] |
rs6006317 | 1.00[AMR][1000 genomes] |
rs6006318 | 1.00[AMR][1000 genomes] |
rs6006331 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60964812 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs61043203 | 1.00[AMR][1000 genomes] |
rs61191536 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73396842 | 1.00[AMR][1000 genomes] |
rs73396845 | 1.00[AMR][1000 genomes] |
rs73398604 | 1.00[AMR][1000 genomes] |
rs73398637 | 1.00[AMR][1000 genomes] |
rs73398640 | 1.00[AMR][1000 genomes] |
rs73398663 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73400621 | 0.83[AMR][1000 genomes] |
rs73400633 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73400648 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73400675 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73400689 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73402627 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73402640 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73402644 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73402647 | 1.00[AMR][1000 genomes] |
rs73402653 | 1.00[AMR][1000 genomes] |
rs73402667 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9620939 | 0.83[AMR][1000 genomes] |
rs9625903 | 0.83[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1064081 | chr22:29826745-30623965 | Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
2 | nsv544677 | chr22:29826745-30623965 | Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
3 | nsv588884 | chr22:30494371-30590026 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv834173 | chr22:30515092-30658277 | Enhancers ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
5 | nsv527188 | chr22:30529741-30581722 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv966100 | chr22:30530653-30547684 | Weak transcription Enhancers ZNF genes & repeats | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr22:30540200-30541000 | Enhancers | K562 | blood |