Variant report
Variant | rs907490 |
---|---|
Chromosome Location | chr3:145989839-145989840 |
allele | A/G |
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] |
---|---|
rs10737947 | 0.84[EUR][1000 genomes] |
rs10804710 | 0.89[EUR][1000 genomes] |
rs10935613 | 0.87[EUR][1000 genomes] |
rs10935614 | 0.89[EUR][1000 genomes] |
rs10935615 | 0.89[EUR][1000 genomes] |
rs10935616 | 0.89[EUR][1000 genomes] |
rs11709096 | 0.89[EUR][1000 genomes] |
rs11915448 | 0.87[EUR][1000 genomes] |
rs11919011 | 0.89[EUR][1000 genomes] |
rs12633074 | 0.89[EUR][1000 genomes] |
rs1355570 | 0.97[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1398122 | 0.81[ASN][1000 genomes] |
rs1398125 | 0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1512078 | 0.86[EUR][1000 genomes] |
rs1512079 | 0.89[EUR][1000 genomes] |
rs1512081 | 0.89[EUR][1000 genomes] |
rs1512890 | 0.81[EUR][1000 genomes] |
rs1877511 | 0.87[EUR][1000 genomes] |
rs2175544 | 0.84[EUR][1000 genomes] |
rs2175545 | 0.89[EUR][1000 genomes] |
rs2867081 | 0.87[EUR][1000 genomes] |
rs2867083 | 0.86[EUR][1000 genomes] |
rs2867084 | 0.90[EUR][1000 genomes] |
rs2903479 | 0.87[EUR][1000 genomes] |
rs4273339 | 0.87[EUR][1000 genomes] |
rs4488802 | 0.89[EUR][1000 genomes] |
rs4681306 | 0.86[EUR][1000 genomes] |
rs4681307 | 0.89[EUR][1000 genomes] |
rs4681308 | 0.89[EUR][1000 genomes] |
rs6440422 | 0.87[EUR][1000 genomes] |
rs6775520 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6792732 | 0.89[EUR][1000 genomes] |
rs6800307 | 0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6805377 | 0.89[EUR][1000 genomes] |
rs7430290 | 0.89[EUR][1000 genomes] |
rs7621841 | 0.89[EUR][1000 genomes] |
rs7632412 | 0.89[EUR][1000 genomes] |
rs7634568 | 0.89[EUR][1000 genomes] |
rs7643778 | 0.89[EUR][1000 genomes] |
rs7645100 | 0.94[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9289719 | 0.88[ASN][1000 genomes] |
rs9813122 | 0.86[EUR][1000 genomes] |
rs9825776 | 0.89[EUR][1000 genomes] |
rs9826132 | 0.89[EUR][1000 genomes] |
rs9826360 | 0.89[EUR][1000 genomes] |
rs9838866 | 0.81[EUR][1000 genomes] |
rs9845890 | 0.86[EUR][1000 genomes] |
rs9851511 | 0.87[EUR][1000 genomes] |
rs9855695 | 0.89[EUR][1000 genomes] |
rs9863647 | 0.87[EUR][1000 genomes] |
rs9867851 | 0.88[EUR][1000 genomes] |
rs9875799 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877614 | chr3:145903426-146025896 | ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
2 | esv3333601 | chr3:145940702-146068210 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | esv3416330 | chr3:145941029-146068457 | Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv998388 | chr3:145960954-146087749 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:145983800-145998800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr3:145984600-145990000 | Weak transcription | H9 Cell Line | embryonic stem cell |
3 | chr3:145987000-145991800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
4 | chr3:145987000-145992000 | Weak transcription | Muscle Satellite Cultured Cells | -- |