Variant report
| Variant | rs569407 |
|---|---|
| Chromosome Location | chr1:166627327-166627328 |
| allele | C/T |
| 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 |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000234984 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:30)
| rs_ID | r2[population] |
|---|---|
| rs1372683 | 0.87[EUR][1000 genomes] |
| rs1372684 | 0.87[EUR][1000 genomes] |
| rs1561844 | 0.87[EUR][1000 genomes] |
| rs1899440 | 0.87[EUR][1000 genomes] |
| rs479799 | 0.87[EUR][1000 genomes] |
| rs486610 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs487459 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs488358 | 0.81[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs488426 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs489060 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
| rs489144 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
| rs491814 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs496879 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
| rs503909 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs509587 | 0.87[EUR][1000 genomes] |
| rs513797 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs513884 | 0.84[EUR][1000 genomes] |
| rs516754 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes] |
| rs521580 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs528088 | 0.85[AMR][1000 genomes];0.93[EUR][1000 genomes] |
| rs529293 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs534733 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs539458 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
| rs539548 | 0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes] |
| rs549764 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs565064 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
| rs565418 | 0.95[AFR][1000 genomes] |
| rs566146 | 0.87[EUR][1000 genomes] |
| rs579671 | 0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes] |
| rs6682466 | 0.87[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv916491 | chr1:166000783-166948513 | Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
| 2 | esv2757759 | chr1:166491879-166650985 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| 3 | esv2758975 | chr1:166491879-166650985 | ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| 4 | esv2752389 | chr1:166625342-166706342 | Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
