Variant report
Variant | rs73283621 |
---|---|
Chromosome Location | chr10:58130454-58130455 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:58120227..58123041-chr10:58129207..58132105,4 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000122952 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs16908827 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16908833 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16908837 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs58358142 | 1.00[AMR][1000 genomes] |
rs60761978 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73281989 | 1.00[AMR][1000 genomes] |
rs73281991 | 1.00[AMR][1000 genomes] |
rs73281992 | 1.00[AMR][1000 genomes] |
rs73281994 | 1.00[AMR][1000 genomes] |
rs73281997 | 1.00[AMR][1000 genomes] |
rs73281998 | 1.00[AMR][1000 genomes] |
rs73283614 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73283620 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73283625 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73283693 | 1.00[AMR][1000 genomes] |
rs73283823 | 1.00[AMR][1000 genomes] |
rs73285910 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752691 | chr10:57738694-58541894 | Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
2 | nsv831883 | chr10:57947759-58139056 | Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
3 | nsv895503 | chr10:58029209-58201703 | Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
4 | nsv895504 | chr10:58029209-58230622 | Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
5 | nsv1035842 | chr10:58084841-58150135 | Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:58130200-58130600 | Enhancers | K562 | blood |