Variant report
Variant | rs223663 |
---|---|
Chromosome Location | chr2:32017829-32017830 |
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 |
---|---|
ENSG00000223647 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1090829 | 1.00[EUR][1000 genomes] |
rs11682335 | 1.00[AMR][1000 genomes] |
rs13403364 | 1.00[AMR][1000 genomes] |
rs160793 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs160794 | 1.00[EUR][1000 genomes] |
rs160810 | 0.89[EUR][1000 genomes] |
rs2093300 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs221195 | 0.94[EUR][1000 genomes] |
rs223618 | 1.00[EUR][1000 genomes] |
rs223619 | 1.00[EUR][1000 genomes] |
rs223624 | 1.00[EUR][1000 genomes] |
rs223648 | 1.00[EUR][1000 genomes] |
rs223654 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs413895 | 0.94[EUR][1000 genomes] |
rs4141418 | 1.00[EUR][1000 genomes] |
rs533970 | 1.00[AMR][1000 genomes] |
rs631826 | 1.00[AMR][1000 genomes] |
rs648652 | 1.00[AMR][1000 genomes] |
rs6543638 | 1.00[EUR][1000 genomes] |
rs6543639 | 1.00[EUR][1000 genomes] |
rs6708897 | 0.89[EUR][1000 genomes] |
rs7589874 | 0.88[EUR][1000 genomes] |
rs7600278 | 1.00[AMR][1000 genomes] |
rs806149 | 1.00[AMR][1000 genomes] |
rs806595 | 1.00[EUR][1000 genomes] |
rs806596 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532648 | chr2:31591498-32312698 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
2 | esv3376782 | chr2:31861607-32046180 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv1003376 | chr2:31889934-32022595 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv1015021 | chr2:31972738-32030696 | Enhancers Weak transcription | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |