Variant report
Variant | rs2823057 |
---|---|
Chromosome Location | chr21:16474829-16474830 |
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 |
No data |
(count:2 , 50 per page) page:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000180530 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17001407 | 0.94[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17001451 | 0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs17001480 | 0.94[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs8127456 | 0.90[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834048 | chr21:16324481-16489570 | Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv521517 | chr21:16474158-16482643 | Enhancers Weak transcription | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |