Variant report
Variant | rs72925705 |
---|---|
Chromosome Location | chr3:90213771-90213772 |
allele | A/C |
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] |
---|---|
rs11128081 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11917293 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11918512 | 1.00[EUR][1000 genomes] |
rs11920640 | 1.00[EUR][1000 genomes] |
rs11924267 | 1.00[EUR][1000 genomes] |
rs11926877 | 1.00[EUR][1000 genomes] |
rs12106840 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12107978 | 1.00[EUR][1000 genomes] |
rs12107987 | 1.00[EUR][1000 genomes] |
rs1402829 | 1.00[EUR][1000 genomes] |
rs1402830 | 1.00[EUR][1000 genomes] |
rs1402831 | 1.00[EUR][1000 genomes] |
rs1521801 | 1.00[EUR][1000 genomes] |
rs1521805 | 1.00[EUR][1000 genomes] |
rs1915788 | 1.00[EUR][1000 genomes] |
rs1996783 | 1.00[EUR][1000 genomes] |
rs1996784 | 1.00[EUR][1000 genomes] |
rs2204079 | 1.00[EUR][1000 genomes] |
rs55719953 | 1.00[EUR][1000 genomes] |
rs55726199 | 1.00[EUR][1000 genomes] |
rs56257056 | 1.00[EUR][1000 genomes] |
rs56971856 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57237979 | 1.00[EUR][1000 genomes] |
rs57268246 | 1.00[EUR][1000 genomes] |
rs57530512 | 1.00[EUR][1000 genomes] |
rs57742239 | 1.00[EUR][1000 genomes] |
rs57945456 | 1.00[EUR][1000 genomes] |
rs57953580 | 1.00[EUR][1000 genomes] |
rs58442773 | 1.00[EUR][1000 genomes] |
rs58444511 | 1.00[EUR][1000 genomes] |
rs58944054 | 1.00[EUR][1000 genomes] |
rs58977999 | 1.00[EUR][1000 genomes] |
rs59147897 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59297554 | 1.00[EUR][1000 genomes] |
rs59437743 | 1.00[EUR][1000 genomes] |
rs59649185 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59827615 | 1.00[EUR][1000 genomes] |
rs60834002 | 1.00[EUR][1000 genomes] |
rs61037499 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6551449 | 1.00[EUR][1000 genomes] |
rs6770945 | 1.00[EUR][1000 genomes] |
rs6772724 | 1.00[EUR][1000 genomes] |
rs6780268 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6782153 | 1.00[EUR][1000 genomes] |
rs6789628 | 1.00[EUR][1000 genomes] |
rs6789752 | 1.00[EUR][1000 genomes] |
rs6793888 | 1.00[EUR][1000 genomes] |
rs6798554 | 1.00[EUR][1000 genomes] |
rs6800705 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6804358 | 1.00[EUR][1000 genomes] |
rs72921826 | 1.00[EUR][1000 genomes] |
rs72921827 | 1.00[EUR][1000 genomes] |
rs72921828 | 1.00[EUR][1000 genomes] |
rs72921847 | 1.00[EUR][1000 genomes] |
rs72921850 | 1.00[EUR][1000 genomes] |
rs72921853 | 1.00[EUR][1000 genomes] |
rs72921855 | 1.00[EUR][1000 genomes] |
rs72921864 | 1.00[EUR][1000 genomes] |
rs72921866 | 1.00[EUR][1000 genomes] |
rs72921873 | 1.00[EUR][1000 genomes] |
rs72921876 | 1.00[EUR][1000 genomes] |
rs72923735 | 1.00[EUR][1000 genomes] |
rs72923736 | 1.00[EUR][1000 genomes] |
rs72923737 | 1.00[EUR][1000 genomes] |
rs72923739 | 1.00[EUR][1000 genomes] |
rs72923741 | 1.00[EUR][1000 genomes] |
rs72923755 | 1.00[EUR][1000 genomes] |
rs72923757 | 1.00[EUR][1000 genomes] |
rs72923762 | 1.00[EUR][1000 genomes] |
rs72923764 | 1.00[EUR][1000 genomes] |
rs72923765 | 1.00[EUR][1000 genomes] |
rs72923767 | 1.00[EUR][1000 genomes] |
rs72923770 | 1.00[EUR][1000 genomes] |
rs72923771 | 1.00[EUR][1000 genomes] |
rs72923776 | 1.00[EUR][1000 genomes] |
rs72923777 | 1.00[EUR][1000 genomes] |
rs72923779 | 1.00[EUR][1000 genomes] |
rs72923781 | 1.00[EUR][1000 genomes] |
rs72923783 | 0.81[AFR][1000 genomes] |
rs72923784 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72923786 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72923794 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72925712 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72925771 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72925799 | 1.00[EUR][1000 genomes] |
rs73846008 | 1.00[EUR][1000 genomes] |
rs73849912 | 1.00[EUR][1000 genomes] |
rs7610765 | 1.00[EUR][1000 genomes] |
rs7619437 | 1.00[EUR][1000 genomes] |
rs7626330 | 0.81[AFR][1000 genomes] |
rs7627792 | 1.00[EUR][1000 genomes] |
rs7637541 | 1.00[EUR][1000 genomes] |
rs7648089 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7648275 | 0.81[AFR][1000 genomes] |
rs7648900 | 1.00[EUR][1000 genomes] |
rs9818065 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1008018 | chr3:89382031-90254063 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv536639 | chr3:89382031-90254063 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv530024 | chr3:89548440-90304841 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv590970 | chr3:89987871-90441306 | Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv965184 | chr3:90202286-90234890 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS | TF binding region | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:90213000-90213800 | Enhancers | Fetal Lung | lung |
2 | chr3:90213000-90214200 | Strong transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |