Variant report
Variant | rs9859534 |
---|---|
Chromosome Location | chr3:110488423-110488424 |
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] |
---|---|
rs10934065 | 0.82[EUR][1000 genomes] |
rs1156330 | 0.90[EUR][1000 genomes] |
rs1156743 | 0.82[EUR][1000 genomes] |
rs1156744 | 0.81[EUR][1000 genomes] |
rs1156775 | 0.90[EUR][1000 genomes] |
rs1156776 | 0.89[EUR][1000 genomes] |
rs1156777 | 0.90[EUR][1000 genomes] |
rs11715183 | 0.85[EUR][1000 genomes] |
rs1303902 | 0.81[EUR][1000 genomes] |
rs13098266 | 0.84[EUR][1000 genomes] |
rs13098277 | 0.82[EUR][1000 genomes] |
rs1350929 | 0.90[EUR][1000 genomes] |
rs1381604 | 0.97[EUR][1000 genomes] |
rs1462294 | 0.88[EUR][1000 genomes] |
rs1462301 | 0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1462302 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1462303 | 0.89[EUR][1000 genomes] |
rs1462306 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1462314 | 0.82[EUR][1000 genomes] |
rs1462315 | 0.83[EUR][1000 genomes] |
rs1462316 | 0.88[EUR][1000 genomes] |
rs1585559 | 0.95[EUR][1000 genomes] |
rs1599569 | 0.89[EUR][1000 genomes] |
rs1599570 | 0.81[EUR][1000 genomes] |
rs1599572 | 0.81[EUR][1000 genomes] |
rs1599574 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs17202466 | 0.82[EUR][1000 genomes] |
rs1824630 | 0.88[EUR][1000 genomes] |
rs1903678 | 0.89[EUR][1000 genomes] |
rs2054375 | 0.83[EUR][1000 genomes] |
rs2126450 | 0.82[EUR][1000 genomes] |
rs2169496 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2199454 | 0.89[EUR][1000 genomes] |
rs2399356 | 0.87[EUR][1000 genomes] |
rs2399357 | 0.82[EUR][1000 genomes] |
rs2399361 | 0.90[EUR][1000 genomes] |
rs2399362 | 0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4234400 | 0.86[EUR][1000 genomes] |
rs4362750 | 0.86[EUR][1000 genomes] |
rs4395426 | 0.80[EUR][1000 genomes] |
rs4410465 | 0.80[EUR][1000 genomes] |
rs4438690 | 0.89[EUR][1000 genomes] |
rs4481181 | 0.86[EUR][1000 genomes] |
rs4610259 | 0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4634158 | 0.80[EUR][1000 genomes] |
rs4640600 | 0.80[EUR][1000 genomes] |
rs4682018 | 0.86[EUR][1000 genomes] |
rs4682019 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4682020 | 0.87[EUR][1000 genomes] |
rs4682198 | 0.86[EUR][1000 genomes] |
rs4682204 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4682205 | 0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4682206 | 0.89[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs4682207 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs55894328 | 0.87[EUR][1000 genomes] |
rs56203101 | 0.82[EUR][1000 genomes] |
rs6437925 | 0.90[EUR][1000 genomes] |
rs6762150 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6773268 | 0.83[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs6784490 | 0.87[EUR][1000 genomes] |
rs6805801 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6809227 | 0.87[EUR][1000 genomes] |
rs7615772 | 0.89[EUR][1000 genomes] |
rs7629191 | 0.82[EUR][1000 genomes] |
rs7633076 | 0.90[EUR][1000 genomes] |
rs7633234 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7633936 | 0.82[EUR][1000 genomes] |
rs7637286 | 0.80[EUR][1000 genomes] |
rs7640594 | 0.90[EUR][1000 genomes] |
rs7647181 | 0.82[EUR][1000 genomes] |
rs7647421 | 0.81[EUR][1000 genomes] |
rs9288913 | 0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs931019 | 0.83[EUR][1000 genomes] |
rs9816253 | 0.90[EUR][1000 genomes] |
rs9820478 | 0.90[EUR][1000 genomes] |
rs9830854 | 0.82[EUR][1000 genomes] |
rs9830959 | 0.90[EUR][1000 genomes] |
rs9836371 | 0.82[EUR][1000 genomes] |
rs9837589 | 0.82[EUR][1000 genomes] |
rs9838550 | 0.85[EUR][1000 genomes] |
rs9838611 | 0.80[EUR][1000 genomes] |
rs9842924 | 0.89[EUR][1000 genomes] |
rs9857065 | 0.95[EUR][1000 genomes] |
rs9857228 | 0.87[EUR][1000 genomes] |
rs9864306 | 0.80[EUR][1000 genomes] |
rs991930 | 0.95[EUR][1000 genomes] |
rs994125 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1001810 | chr3:110158316-110522247 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1010230 | chr3:110204439-110588814 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv536688 | chr3:110204439-110588814 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1011034 | chr3:110209344-110559021 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv536689 | chr3:110209344-110559021 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv1003106 | chr3:110264476-111105943 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
7 | nsv1014199 | chr3:110293896-110754155 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | nsv829673 | chr3:110378069-110530815 | Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:110471400-110492200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr3:110472600-110492400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr3:110486200-110490000 | Weak transcription | HepG2 | liver |
4 | chr3:110486400-110492200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
5 | chr3:110488000-110490800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |