Variant report
Variant | rs9883836 |
---|---|
Chromosome Location | chr3:24975890-24975891 |
allele | C/T |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:24975006..24977097-chr3:24999784..25002405,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11710017 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs11712813 | 0.83[ASN][1000 genomes] |
rs12330318 | 0.82[AMR][1000 genomes] |
rs12330519 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12629369 | 0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12638313 | 0.86[EUR][1000 genomes] |
rs12715064 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs13098681 | 0.83[AMR][1000 genomes] |
rs2363523 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2363524 | 0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2363525 | 0.88[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs2363526 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2363528 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2363529 | 0.95[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2363530 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs4368469 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs4858667 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6772493 | 0.83[EUR][1000 genomes] |
rs6779838 | 0.90[EUR][1000 genomes] |
rs6798808 | 0.87[EUR][1000 genomes] |
rs7614721 | 0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7614855 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7648839 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9812847 | 0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9833261 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9843826 | 0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9845970 | 0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9847199 | 0.92[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs9872534 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs9878781 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs9881002 | 0.89[ASN][1000 genomes] |
rs9881799 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9882350 | 0.85[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv589953 | chr3:24909003-25004804 | Enhancers Weak transcription Bivalent Enhancer Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv876630 | chr3:24911917-25066711 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv834644 | chr3:24936987-25112610 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv460482 | chr3:24966768-25071616 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv589954 | chr3:24966768-25071616 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
6 | nsv1008974 | chr3:24968434-24992497 | Weak transcription Enhancers Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:24975000-24976000 | Enhancers | Fetal Kidney | kidney |
2 | chr3:24975000-24976000 | Enhancers | Fetal Lung | lung |