Variant report
Variant | rs276440 |
---|---|
Chromosome Location | chr9:15627596-15627597 |
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] |
---|---|
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] |
rs10119980 | 0.94[EUR][1000 genomes] |
rs10120171 | 1.00[ASN][1000 genomes] |
rs10121012 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10121391 | 0.93[EUR][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] |
rs10217374 | 0.90[EUR][1000 genomes] |
rs1039812 | 0.87[EUR][1000 genomes] |
rs1039816 | 0.84[EUR][1000 genomes] |
rs1041529 | 1.00[ASN][1000 genomes] |
rs10733296 | 0.87[EUR][1000 genomes] |
rs10738407 | 0.90[EUR][1000 genomes] |
rs10756706 | 0.81[EUR][1000 genomes] |
rs10962054 | 1.00[ASN][1000 genomes] |
rs10962061 | 1.00[ASN][1000 genomes] |
rs12336383 | 1.00[ASN][1000 genomes] |
rs12336445 | 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] |
rs12350267 | 0.87[EUR][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] |
rs1355172 | 0.87[EUR][1000 genomes] |
rs1509311 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1553727 | 0.94[EUR][1000 genomes] |
rs175762 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1848583 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs202321 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2055773 | 0.87[EUR][1000 genomes] |
rs2055774 | 0.87[EUR][1000 genomes] |
rs2064030 | 1.00[ASN][1000 genomes] |
rs2089618 | 0.90[EUR][1000 genomes] |
rs2136354 | 0.90[EUR][1000 genomes] |
rs2175083 | 0.87[EUR][1000 genomes] |
rs2202865 | 1.00[ASN][1000 genomes] |
rs2221706 | 0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2382531 | 0.93[EUR][1000 genomes] |
rs2382533 | 0.90[EUR][1000 genomes] |
rs2382535 | 0.90[EUR][1000 genomes] |
rs2382536 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs2665515 | 1.00[ASN][1000 genomes] |
rs2737840 | 1.00[ASN][1000 genomes] |
rs276434 | 1.00[ASN][1000 genomes] |
rs276437 | 0.91[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs276438 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs276439 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs276442 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs276445 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs276446 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs276450 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs276451 | 0.86[AFR][1000 genomes];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 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28449490 | 1.00[ASN][1000 genomes] |
rs28497163 | 1.00[ASN][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 | 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] |
rs3119700 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs3122701 | 0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3122705 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3129711 | 0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs365710 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs381205 | 1.00[ASN][1000 genomes] |
rs392627 | 1.00[ASN][1000 genomes] |
rs398117 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs398178 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs399808 | 1.00[ASN][1000 genomes] |
rs401393 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs413356 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs415157 | 1.00[ASN][1000 genomes] |
rs418153 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4237140 | 0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs424131 | 1.00[ASN][1000 genomes] |
rs4445326 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4740623 | 0.90[EUR][1000 genomes] |
rs4741532 | 0.93[EUR][1000 genomes] |
rs4741533 | 0.93[EUR][1000 genomes] |
rs4741536 | 0.84[EUR][1000 genomes] |
rs4741537 | 0.84[EUR][1000 genomes] |
rs592452 | 1.00[ASN][1000 genomes] |
rs6474941 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs6474943 | 0.83[AMR][1000 genomes] |
rs6474947 | 0.93[EUR][1000 genomes] |
rs6474949 | 0.87[EUR][1000 genomes] |
rs6474956 | 0.85[EUR][1000 genomes] |
rs6474957 | 0.90[EUR][1000 genomes] |
rs6474973 | 0.81[EUR][1000 genomes] |
rs7021840 | 1.00[ASN][1000 genomes] |
rs7035422 | 0.97[EUR][1000 genomes] |
rs7037893 | 0.88[EUR][1000 genomes] |
rs7038210 | 0.83[EUR][1000 genomes] |
rs7038920 | 0.90[EUR][1000 genomes] |
rs7847148 | 0.97[EUR][1000 genomes] |
rs7849159 | 0.87[EUR][1000 genomes] |
rs7852936 | 1.00[ASN][1000 genomes] |
rs7860339 | 1.00[ASN][1000 genomes] |
rs7865193 | 0.84[EUR][1000 genomes] |
rs7870315 | 0.94[EUR][1000 genomes] |
rs796391 | 0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs811282 | 1.00[ASN][1000 genomes] |
rs926154 | 1.00[ASN][1000 genomes] |
rs9298734 | 0.93[EUR][1000 genomes] |
rs9406518 | 1.00[ASN][1000 genomes] |
rs9919009 | 0.81[EUR][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 | 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 |
8 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | nsv613654 | chr9:15601971-15638364 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
13 | nsv613655 | chr9:15602101-15670445 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
14 | nsv892633 | chr9:15604746-15889411 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
15 | nsv613656 | chr9:15615321-15696501 | Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | nsv466262 | chr9:15615321-15727518 | ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
17 | nsv613657 | chr9:15615321-15727518 | ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
18 | nsv969752 | chr9:15615716-15639356 | Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:15611200-15628200 | Weak transcription | Thymus | Thymus |
2 | chr9:15614200-15629800 | Weak transcription | Fetal Lung | lung |
3 | chr9:15614400-15645000 | Weak transcription | Primary hematopoietic stem cells | blood |
4 | chr9:15618200-15628200 | Weak transcription | Fetal Stomach | stomach |
5 | chr9:15618400-15627600 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
6 | chr9:15618800-15629000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
7 | chr9:15625000-15635400 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |