Variant report
| Variant | rs13052106 |
|---|---|
| Chromosome Location | chr21:16922750-16922751 |
| allele | A/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:
1
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000180530 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:24)
| rs_ID | r2[population] |
|---|---|
| rs1076605 | 0.83[AFR][1000 genomes] |
| rs1076606 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
| rs10854388 | 0.84[AFR][1000 genomes];0.96[ASN][1000 genomes] |
| rs13051322 | 0.92[EUR][1000 genomes] |
| rs2003648 | 0.92[AFR][1000 genomes];0.93[EUR][1000 genomes] |
| rs2150373 | 0.90[AFR][1000 genomes];0.95[ASN][1000 genomes] |
| rs2179030 | 0.86[ASN][1000 genomes] |
| rs2823343 | 0.85[ASN][1000 genomes] |
| rs2823361 | 0.83[AFR][1000 genomes] |
| rs2823363 | 0.99[AFR][1000 genomes];1.00[EUR][1000 genomes] |
| rs4594532 | 0.87[AFR][1000 genomes];0.86[ASN][1000 genomes] |
| rs4817962 | 0.83[AFR][1000 genomes];0.95[ASN][1000 genomes] |
| rs4817964 | 0.95[ASN][1000 genomes] |
| rs7277940 | 0.92[EUR][1000 genomes] |
| rs7278086 | 0.81[AFR][1000 genomes] |
| rs7279770 | 0.98[ASN][1000 genomes] |
| rs7280990 | 0.87[AFR][1000 genomes];0.95[ASN][1000 genomes] |
| rs7283418 | 0.92[EUR][1000 genomes] |
| rs9974040 | 0.85[AFR][1000 genomes];0.94[ASN][1000 genomes] |
| rs9974396 | 0.85[AFR][1000 genomes];0.95[ASN][1000 genomes] |
| rs9974659 | 0.87[AFR][1000 genomes];0.95[ASN][1000 genomes] |
| rs9976620 | 0.85[AFR][1000 genomes] |
| rs9981901 | 0.86[ASN][1000 genomes] |
| rs9982379 | 0.87[AFR][1000 genomes];0.86[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1063385 | chr21:16521617-16926212 | Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| 2 | nsv1064280 | chr21:16664312-17049272 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| 3 | nsv1064621 | chr21:16881027-16937290 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
| 4 | esv2758530 | chr21:16912646-17096678 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| 5 | esv2758810 | chr21:16912646-17096678 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription | TF binding regionChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
