Variant report
Variant | rs4683484 |
---|---|
Chromosome Location | chr3:139987821-139987822 |
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 | chr3:139985294..139989044-chr3:139992240..139995969,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11717522 | 1.00[JPT][hapmap] |
rs11917245 | 1.00[JPT][hapmap] |
rs13319247 | 1.00[JPT][hapmap] |
rs1383020 | 1.00[JPT][hapmap] |
rs1479866 | 1.00[JPT][hapmap] |
rs1564395 | 1.00[JPT][hapmap] |
rs1564397 | 1.00[JPT][hapmap] |
rs2061927 | 1.00[JPT][hapmap] |
rs2061929 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2086330 | 1.00[JPT][hapmap] |
rs3943277 | 1.00[JPT][hapmap] |
rs4076964 | 1.00[JPT][hapmap] |
rs4362682 | 1.00[JPT][hapmap];0.89[ASN][1000 genomes] |
rs4365587 | 1.00[JPT][hapmap];0.89[ASN][1000 genomes] |
rs4371479 | 0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs4423726 | 0.83[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4438621 | 1.00[JPT][hapmap] |
rs4518083 | 1.00[JPT][hapmap] |
rs4583599 | 1.00[JPT][hapmap] |
rs4683488 | 1.00[JPT][hapmap] |
rs4683817 | 0.83[ASN][1000 genomes] |
rs60094335 | 0.89[ASN][1000 genomes] |
rs62267960 | 0.83[ASN][1000 genomes] |
rs6439912 | 0.89[ASN][1000 genomes] |
rs6765022 | 1.00[CHB][hapmap] |
rs6765087 | 1.00[JPT][hapmap] |
rs6782976 | 0.89[ASN][1000 genomes] |
rs6789431 | 0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.83[ASN][1000 genomes] |
rs71314547 | 0.83[EUR][1000 genomes] |
rs73867103 | 0.89[ASN][1000 genomes] |
rs73867105 | 0.89[ASN][1000 genomes] |
rs73867110 | 0.89[ASN][1000 genomes] |
rs7431715 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs967861 | 1.00[CHB][hapmap] |
rs9811609 | 1.00[JPT][hapmap];0.85[YRI][hapmap] |
rs9817769 | 1.00[JPT][hapmap] |
rs9840502 | 0.83[ASN][1000 genomes] |
rs9844835 | 0.91[CEU][hapmap] |
rs9846393 | 0.83[ASN][1000 genomes] |
rs9861445 | 0.84[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs995578 | 1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv829739 | chr3:139797496-140002685 | Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv432486 | chr3:139924092-140049121 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | esv2757891 | chr3:139925764-140524730 | Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
4 | esv2759181 | chr3:139925764-140524730 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
5 | nsv829740 | chr3:139925767-140106169 | Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv527831 | chr3:139932966-140533823 | Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:139980200-139999400 | Weak transcription | Pancreas | Pancrea |
2 | chr3:139981200-139989000 | Weak transcription | Spleen | Spleen |
3 | chr3:139984400-139992800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |