Variant report
Variant | rs10470570 |
---|---|
Chromosome Location | chr3:86749619-86749620 |
allele | G/T |
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] |
---|---|
rs11127959 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11714652 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11718975 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs11917335 | 0.86[EUR][1000 genomes] |
rs11919691 | 0.90[EUR][1000 genomes] |
rs12489293 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12489298 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12489313 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12493521 | 0.87[EUR][1000 genomes] |
rs12495229 | 0.82[EUR][1000 genomes] |
rs12495954 | 0.84[EUR][1000 genomes] |
rs1370209 | 0.92[EUR][1000 genomes] |
rs1370210 | 0.92[EUR][1000 genomes] |
rs1370212 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1437047 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs1437049 | 0.84[EUR][1000 genomes] |
rs1437055 | 0.86[EUR][1000 genomes] |
rs1583577 | 0.84[EUR][1000 genomes] |
rs1583578 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs17364877 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs2011715 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2043685 | 0.87[EUR][1000 genomes] |
rs2083018 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2118188 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2118189 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2118191 | 0.87[EUR][1000 genomes] |
rs2118192 | 0.86[EUR][1000 genomes] |
rs2164647 | 0.85[EUR][1000 genomes] |
rs2324795 | 0.87[EUR][1000 genomes] |
rs28453822 | 0.84[EUR][1000 genomes] |
rs28553515 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs28894812 | 0.87[EUR][1000 genomes] |
rs35309716 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs36015800 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4425259 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4572769 | 0.87[EUR][1000 genomes] |
rs4855148 | 0.87[EUR][1000 genomes] |
rs4855174 | 0.87[EUR][1000 genomes] |
rs55711545 | 0.88[EUR][1000 genomes] |
rs55719700 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs56044242 | 0.86[EUR][1000 genomes] |
rs6775872 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6777551 | 0.92[EUR][1000 genomes] |
rs6779214 | 0.87[EUR][1000 genomes] |
rs6782806 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6807530 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs728180 | 0.84[EUR][1000 genomes] |
rs73133829 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs73137958 | 0.87[EUR][1000 genomes] |
rs73137985 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs73139911 | 0.86[EUR][1000 genomes] |
rs73139914 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs73139922 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs73139923 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7630849 | 0.86[EUR][1000 genomes] |
rs7631441 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs920188 | 0.87[EUR][1000 genomes] |
rs9631517 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9756254 | 0.90[EUR][1000 genomes] |
rs9815344 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs9815450 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs9818400 | 0.84[EUR][1000 genomes] |
rs9821486 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9833108 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9841059 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9844776 | 0.86[EUR][1000 genomes] |
rs9858679 | 0.81[EUR][1000 genomes] |
rs9859483 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9862624 | 0.90[EUR][1000 genomes] |
rs9864625 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9866183 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9881535 | 0.87[EUR][1000 genomes] |
rs9985323 | 0.98[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs9985324 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877116 | chr3:86518318-86964922 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
2 | esv1829775 | chr3:86534927-86822085 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
3 | nsv877117 | chr3:86665408-86927574 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | esv1794028 | chr3:86684769-86822085 | Enhancers Active TSS Weak transcription ZNF genes & repeats | lncRNA | 11 gene(s) | inside rSNPs | n/a |
5 | esv1827728 | chr3:86684769-86822085 | Enhancers Weak transcription ZNF genes & repeats Active TSS | lncRNA | 11 gene(s) | inside rSNPs | n/a |
6 | nsv1005747 | chr3:86701703-86792434 | Enhancers Active TSS ZNF genes & repeats Weak transcription | lncRNA | 11 gene(s) | inside rSNPs | n/a |
7 | nsv536630 | chr3:86701703-86792434 | Weak transcription ZNF genes & repeats Enhancers Active TSS | lncRNA | 11 gene(s) | inside rSNPs | n/a |
8 | nsv999877 | chr3:86704171-86795449 | Enhancers Active TSS Weak transcription ZNF genes & repeats | lncRNA | 11 gene(s) | inside rSNPs | n/a |
9 | nsv527690 | chr3:86711294-86794501 | Weak transcription Enhancers ZNF genes & repeats Active TSS | lncRNA | 10 gene(s) | inside rSNPs | n/a |
10 | nsv877118 | chr3:86722823-86927574 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
11 | nsv877119 | chr3:86722823-86952516 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
12 | nsv877120 | chr3:86722823-86961118 | Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
13 | nsv818155 | chr3:86732817-86752414 | Enhancers Weak transcription Active TSS | n/a | n/a | inside rSNPs | n/a |
14 | nsv877121 | chr3:86732817-86916882 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
15 | nsv877122 | chr3:86732817-86927574 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
16 | nsv877123 | chr3:86732817-86952516 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:86743800-86749800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |