Variant report
Variant | rs1120243 |
---|---|
Chromosome Location | chr20:14162228-14162229 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1033860 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs1118572 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs1980702 | 1.00[AMR][1000 genomes] |
rs204623 | 1.00[AMR][1000 genomes] |
rs204624 | 1.00[AMR][1000 genomes] |
rs2327828 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs2423771 | 1.00[AMR][1000 genomes] |
rs2423776 | 1.00[AMR][1000 genomes] |
rs3121496 | 1.00[AMR][1000 genomes] |
rs3848782 | 1.00[YRI][hapmap] |
rs3909059 | 1.00[YRI][hapmap] |
rs3909060 | 1.00[YRI][hapmap] |
rs3936951 | 1.00[YRI][hapmap] |
rs4814280 | 1.00[YRI][hapmap] |
rs4814281 | 1.00[YRI][hapmap] |
rs4814286 | 1.00[YRI][hapmap] |
rs6033863 | 1.00[YRI][hapmap] |
rs6033874 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs6033875 | 1.00[AMR][1000 genomes] |
rs6033900 | 1.00[AMR][1000 genomes] |
rs6042465 | 1.00[AMR][1000 genomes] |
rs6042467 | 1.00[YRI][hapmap] |
rs6042481 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs6042482 | 1.00[AMR][1000 genomes] |
rs6042504 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs6042540 | 1.00[AMR][1000 genomes] |
rs6042546 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs6042580 | 1.00[AFR][1000 genomes] |
rs6042587 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs6074691 | 1.00[YRI][hapmap] |
rs6079320 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs6079343 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6079347 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6079348 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6105218 | 1.00[YRI][hapmap] |
rs927564 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1066810 | chr20:13451869-14432454 | Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv531479 | chr20:13632491-14434432 | Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
3 | nsv585438 | chr20:14054163-14171905 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1057486 | chr20:14077828-14469129 | ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv1058887 | chr20:14080114-14173534 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv532514 | chr20:14097780-14288315 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |