Variant report
Variant | rs9406518 |
---|---|
Chromosome Location | chr9:15597849-15597850 |
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] |
---|---|
rs10116904 | 1.00[ASN][1000 genomes] |
rs10117524 | 1.00[ASN][1000 genomes] |
rs10118595 | 1.00[ASN][1000 genomes] |
rs10118675 | 1.00[ASN][1000 genomes] |
rs10119257 | 1.00[ASN][1000 genomes] |
rs10119931 | 1.00[ASN][1000 genomes] |
rs10120171 | 1.00[ASN][1000 genomes] |
rs10121012 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10121911 | 1.00[ASN][1000 genomes] |
rs10121971 | 1.00[ASN][1000 genomes] |
rs10123084 | 1.00[ASN][1000 genomes] |
rs10124718 | 1.00[ASN][1000 genomes] |
rs10124746 | 1.00[ASN][1000 genomes] |
rs1041529 | 1.00[ASN][1000 genomes] |
rs10962054 | 1.00[ASN][1000 genomes] |
rs10962061 | 1.00[ASN][1000 genomes] |
rs12336383 | 0.91[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12336445 | 0.91[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12337310 | 1.00[ASN][1000 genomes] |
rs12344963 | 1.00[ASN][1000 genomes] |
rs12348561 | 1.00[ASN][1000 genomes] |
rs12348564 | 1.00[ASN][1000 genomes] |
rs12348780 | 1.00[ASN][1000 genomes] |
rs12350062 | 1.00[ASN][1000 genomes] |
rs12350903 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12352398 | 1.00[ASN][1000 genomes] |
rs12353048 | 1.00[ASN][1000 genomes] |
rs175762 | 1.00[ASN][1000 genomes] |
rs202321 | 1.00[ASN][1000 genomes] |
rs2064030 | 1.00[ASN][1000 genomes] |
rs2202865 | 0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs2665515 | 1.00[ASN][1000 genomes] |
rs2737840 | 1.00[ASN][1000 genomes] |
rs276434 | 1.00[ASN][1000 genomes] |
rs276437 | 1.00[ASN][1000 genomes] |
rs276438 | 1.00[ASN][1000 genomes] |
rs276439 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs276440 | 1.00[ASN][1000 genomes] |
rs276442 | 1.00[ASN][1000 genomes] |
rs276445 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs276446 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs276450 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs276451 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs2777951 | 1.00[ASN][1000 genomes] |
rs2795125 | 1.00[ASN][1000 genomes] |
rs2795128 | 1.00[ASN][1000 genomes] |
rs2821525 | 1.00[ASN][1000 genomes] |
rs2821529 | 1.00[ASN][1000 genomes] |
rs2821542 | 1.00[ASN][1000 genomes] |
rs2821543 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs2821544 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28449490 | 1.00[ASN][1000 genomes] |
rs28497163 | 1.00[ASN][1000 genomes] |
rs28659858 | 0.91[AMR][1000 genomes] |
rs28796681 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28800775 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28805077 | 0.92[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28808908 | 1.00[ASN][1000 genomes] |
rs28844368 | 1.00[ASN][1000 genomes] |
rs28882210 | 1.00[ASN][1000 genomes] |
rs28893033 | 1.00[ASN][1000 genomes] |
rs2891001 | 0.88[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs3119700 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs3122701 | 1.00[ASN][1000 genomes] |
rs3122705 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs3129711 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs365710 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs381205 | 1.00[ASN][1000 genomes] |
rs392627 | 0.91[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs398117 | 1.00[ASN][1000 genomes] |
rs398178 | 1.00[ASN][1000 genomes] |
rs399808 | 0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs401393 | 1.00[ASN][1000 genomes] |
rs413356 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs415157 | 1.00[ASN][1000 genomes] |
rs418153 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs424131 | 1.00[ASN][1000 genomes] |
rs592452 | 1.00[ASN][1000 genomes] |
rs7021840 | 1.00[ASN][1000 genomes] |
rs7852936 | 1.00[ASN][1000 genomes] |
rs7860339 | 1.00[ASN][1000 genomes] |
rs796391 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs811282 | 1.00[ASN][1000 genomes] |
rs926154 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv892625 | chr9:15326251-16064850 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
2 | nsv892626 | chr9:15389610-15694690 | Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
3 | nsv892627 | chr9:15397969-15909450 | Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
4 | nsv892629 | chr9:15516375-15634326 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
5 | esv3407839 | chr9:15530438-15665653 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
6 | nsv892630 | chr9:15554960-15694690 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv1028357 | chr9:15565670-15622556 | Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | esv2752286 | chr9:15578017-15794897 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
9 | nsv613652 | chr9:15579744-15661859 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv613653 | chr9:15590116-15668606 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
11 | nsv892631 | chr9:15590116-15694690 | Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
12 | nsv892632 | chr9:15590116-15869845 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:15587000-15620400 | Weak transcription | Pancreas | Pancrea |
2 | chr9:15588600-15600800 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
3 | chr9:15588600-15601000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
4 | chr9:15589200-15609800 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
5 | chr9:15589400-15610600 | Weak transcription | Thymus | Thymus |
6 | chr9:15592800-15600600 | Weak transcription | Fetal Thymus | thymus |
7 | chr9:15592800-15614000 | Weak transcription | Left Ventricle | heart |
8 | chr9:15593000-15600800 | Weak transcription | H1 Cell Line | embryonic stem cell |
9 | chr9:15595800-15599000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |