Variant report
Variant | rs1554564 |
---|---|
Chromosome Location | chr3:138901333-138901334 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:138899218..138902119-chr3:138905837..138907445,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10935312 | 1.00[ASN][1000 genomes] |
rs11706018 | 0.83[ASN][1000 genomes] |
rs11707723 | 1.00[ASN][1000 genomes] |
rs11719269 | 1.00[ASN][1000 genomes] |
rs11927735 | 1.00[ASN][1000 genomes] |
rs12629175 | 0.83[ASN][1000 genomes] |
rs12629248 | 0.83[ASN][1000 genomes] |
rs12629439 | 0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12630223 | 0.82[ASN][1000 genomes] |
rs12630262 | 0.83[ASN][1000 genomes] |
rs12630333 | 0.83[ASN][1000 genomes] |
rs12631401 | 0.92[ASN][1000 genomes] |
rs12632107 | 0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes] |
rs12632125 | 0.95[ASN][1000 genomes] |
rs12633735 | 0.85[AMR][1000 genomes] |
rs12635620 | 0.83[ASN][1000 genomes] |
rs12636332 | 0.83[ASN][1000 genomes] |
rs12636430 | 0.83[ASN][1000 genomes] |
rs12639194 | 0.93[ASN][1000 genomes] |
rs13067012 | 0.95[ASN][1000 genomes] |
rs13069778 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs13075082 | 1.00[ASN][1000 genomes] |
rs13079289 | 1.00[ASN][1000 genomes] |
rs13079437 | 1.00[ASN][1000 genomes] |
rs13089589 | 0.97[ASN][1000 genomes] |
rs13097708 | 1.00[ASN][1000 genomes] |
rs1554563 | 0.99[ASN][1000 genomes] |
rs1554565 | 1.00[ASN][1000 genomes] |
rs2737737 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs35781224 | 1.00[ASN][1000 genomes] |
rs4365652 | 0.97[ASN][1000 genomes] |
rs4429660 | 1.00[ASN][1000 genomes] |
rs4894383 | 0.96[ASN][1000 genomes] |
rs4894384 | 0.98[ASN][1000 genomes] |
rs56729627 | 1.00[ASN][1000 genomes] |
rs57272617 | 0.80[ASN][1000 genomes] |
rs57678437 | 0.83[ASN][1000 genomes] |
rs6775443 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6778179 | 0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6778394 | 0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73865838 | 0.83[ASN][1000 genomes] |
rs73865842 | 0.83[ASN][1000 genomes] |
rs73868514 | 0.83[ASN][1000 genomes] |
rs73868515 | 0.83[ASN][1000 genomes] |
rs7426421 | 0.99[ASN][1000 genomes] |
rs7614968 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7615670 | 1.00[ASN][1000 genomes] |
rs7623750 | 0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes] |
rs7626912 | 0.97[ASN][1000 genomes] |
rs7627087 | 0.97[ASN][1000 genomes] |
rs7637464 | 1.00[ASN][1000 genomes] |
rs7639780 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv829736 | chr3:138737352-138934758 | Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv1005167 | chr3:138854490-138988546 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv536728 | chr3:138854490-138988546 | Enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:138899800-138905200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr3:138900200-138905200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr3:138901000-138903600 | Enhancers | Primary neutrophils fromperipheralblood | blood |