Variant report
Variant | rs10963012 |
---|---|
Chromosome Location | chr9:17295541-17295542 |
allele | C/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] |
---|---|
rs10114324 | 0.92[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs10120733 | 0.82[ASN][1000 genomes] |
rs1023778 | 0.86[ASN][1000 genomes] |
rs10465046 | 0.81[ASN][1000 genomes] |
rs10756861 | 0.99[ASN][1000 genomes] |
rs10756862 | 0.99[ASN][1000 genomes] |
rs10756863 | 0.93[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs10756864 | 0.97[ASN][1000 genomes] |
rs10756865 | 0.92[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs10810753 | 0.97[ASN][1000 genomes] |
rs10962918 | 0.82[ASN][1000 genomes] |
rs10962922 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs10962923 | 0.82[ASN][1000 genomes] |
rs10962924 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs10962925 | 0.85[AFR][1000 genomes];0.81[ASN][1000 genomes] |
rs10962926 | 0.83[ASN][1000 genomes] |
rs10962927 | 0.83[ASN][1000 genomes] |
rs10962928 | 0.85[ASN][1000 genomes] |
rs10962932 | 0.86[ASN][1000 genomes] |
rs10962933 | 0.86[ASN][1000 genomes] |
rs10962938 | 0.86[ASN][1000 genomes] |
rs10962939 | 0.86[ASN][1000 genomes] |
rs10962940 | 0.86[ASN][1000 genomes] |
rs10962941 | 0.86[ASN][1000 genomes] |
rs10962942 | 0.86[ASN][1000 genomes] |
rs10962960 | 0.86[ASN][1000 genomes] |
rs10962961 | 0.83[AFR][1000 genomes] |
rs10962962 | 0.83[AFR][1000 genomes] |
rs10962963 | 0.83[AFR][1000 genomes] |
rs10962964 | 0.83[AFR][1000 genomes] |
rs10962965 | 0.82[AFR][1000 genomes] |
rs10962977 | 0.88[ASN][1000 genomes] |
rs10962979 | 0.94[ASN][1000 genomes] |
rs10962981 | 0.92[ASN][1000 genomes] |
rs10962983 | 0.89[ASN][1000 genomes] |
rs10962984 | 0.95[ASN][1000 genomes] |
rs10962985 | 0.86[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs10962986 | 0.85[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs10962987 | 0.90[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs10962989 | 0.88[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs10963010 | 0.98[ASN][1000 genomes] |
rs10963011 | 0.89[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10963013 | 1.00[ASN][1000 genomes] |
rs10963014 | 1.00[ASN][1000 genomes] |
rs10963028 | 0.97[ASN][1000 genomes] |
rs1113379 | 0.97[ASN][1000 genomes] |
rs1113380 | 0.97[ASN][1000 genomes] |
rs1113382 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs11525918 | 0.86[ASN][1000 genomes] |
rs11531656 | 0.86[ASN][1000 genomes] |
rs11534160 | 0.85[ASN][1000 genomes] |
rs11536700 | 0.85[AFR][1000 genomes] |
rs11543981 | 0.84[ASN][1000 genomes] |
rs11543983 | 0.93[AFR][1000 genomes] |
rs11562139 | 0.86[ASN][1000 genomes] |
rs12000610 | 0.86[ASN][1000 genomes] |
rs12235987 | 0.85[ASN][1000 genomes] |
rs12237892 | 0.86[ASN][1000 genomes] |
rs12238753 | 0.86[ASN][1000 genomes] |
rs13288412 | 0.85[ASN][1000 genomes] |
rs13289731 | 0.85[ASN][1000 genomes] |
rs1348279 | 0.92[ASN][1000 genomes] |
rs1413418 | 0.87[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1413419 | 0.80[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs1576958 | 0.86[ASN][1000 genomes] |
rs1576959 | 0.86[ASN][1000 genomes] |
rs1576960 | 0.80[AFR][1000 genomes] |
rs1582029 | 0.86[ASN][1000 genomes] |
rs1759452 | 0.94[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759453 | 0.96[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759457 | 0.99[ASN][1000 genomes] |
rs1759458 | 0.99[ASN][1000 genomes] |
rs1759459 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759460 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759461 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759462 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759463 | 0.99[ASN][1000 genomes] |
rs1759465 | 0.99[ASN][1000 genomes] |
rs1759616 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759617 | 0.93[AFR][1000 genomes];0.98[ASN][1000 genomes] |
rs1759619 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1759626 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1819484 | 0.86[ASN][1000 genomes] |
rs1930639 | 0.95[ASN][1000 genomes] |
rs1930643 | 0.93[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs1930644 | 0.97[ASN][1000 genomes] |
rs1930645 | 0.99[ASN][1000 genomes] |
rs1930646 | 0.99[ASN][1000 genomes] |
rs1930647 | 0.82[ASN][1000 genomes] |
rs2010086 | 0.86[ASN][1000 genomes] |
rs2083695 | 0.88[ASN][1000 genomes] |
rs2095145 | 0.88[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2099859 | 0.88[ASN][1000 genomes] |
rs2104914 | 0.81[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2165688 | 0.86[ASN][1000 genomes] |
rs2210551 | 0.83[ASN][1000 genomes] |
rs2383010 | 0.83[AFR][1000 genomes] |
rs2483208 | 1.00[ASN][1000 genomes] |
rs2779774 | 0.95[ASN][1000 genomes] |
rs2779779 | 0.99[ASN][1000 genomes] |
rs2780204 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs2780205 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs2780207 | 0.96[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs2891110 | 0.83[AFR][1000 genomes] |
rs2990958 | 1.00[ASN][1000 genomes] |
rs3808785 | 0.95[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs3814137 | 0.84[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs3814138 | 0.85[AFR][1000 genomes];0.87[ASN][1000 genomes] |
rs3814139 | 0.85[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs3891457 | 0.90[ASN][1000 genomes] |
rs4147023 | 0.80[ASN][1000 genomes] |
rs4430173 | 0.86[ASN][1000 genomes] |
rs4621917 | 0.97[ASN][1000 genomes] |
rs4961537 | 0.86[ASN][1000 genomes] |
rs4961551 | 0.86[ASN][1000 genomes] |
rs4961554 | 0.88[ASN][1000 genomes] |
rs55829722 | 0.85[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs57290709 | 0.87[AFR][1000 genomes] |
rs57750931 | 0.80[AFR][1000 genomes] |
rs57850734 | 0.92[ASN][1000 genomes] |
rs582134 | 0.95[ASN][1000 genomes] |
rs585682 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs593552 | 0.95[ASN][1000 genomes] |
rs599626 | 0.94[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs600041 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs600133 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs601960 | 1.00[ASN][1000 genomes] |
rs606382 | 1.00[ASN][1000 genomes] |
rs60691286 | 0.90[AFR][1000 genomes] |
rs610175 | 0.95[ASN][1000 genomes] |
rs613966 | 1.00[ASN][1000 genomes] |
rs614412 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs614471 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs619357 | 0.96[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs622392 | 0.82[ASN][1000 genomes] |
rs631300 | 0.96[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs632176 | 0.96[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs632255 | 0.89[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs632313 | 0.94[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs634383 | 0.96[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs634446 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs636093 | 0.95[ASN][1000 genomes] |
rs642582 | 0.96[ASN][1000 genomes] |
rs643776 | 0.94[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs646025 | 0.99[ASN][1000 genomes] |
rs647013 | 0.94[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs6475122 | 0.86[ASN][1000 genomes] |
rs6475124 | 0.86[ASN][1000 genomes] |
rs6475125 | 0.86[ASN][1000 genomes] |
rs6475127 | 0.93[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs6475128 | 0.90[AFR][1000 genomes] |
rs6475129 | 0.92[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs664447 | 0.93[ASN][1000 genomes] |
rs672799 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs673587 | 1.00[ASN][1000 genomes] |
rs677490 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs679666 | 0.94[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs7018523 | 0.82[ASN][1000 genomes] |
rs7018856 | 0.84[AFR][1000 genomes];0.92[ASN][1000 genomes] |
rs7020918 | 0.86[ASN][1000 genomes] |
rs7021738 | 0.82[ASN][1000 genomes] |
rs7025912 | 0.85[ASN][1000 genomes] |
rs7027051 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7027539 | 0.88[ASN][1000 genomes] |
rs7034768 | 0.86[ASN][1000 genomes] |
rs7035318 | 0.86[ASN][1000 genomes] |
rs7035386 | 0.86[ASN][1000 genomes] |
rs7035525 | 0.86[ASN][1000 genomes] |
rs7037019 | 0.83[ASN][1000 genomes] |
rs7037041 | 0.86[ASN][1000 genomes] |
rs7037408 | 0.86[ASN][1000 genomes] |
rs7040098 | 0.85[ASN][1000 genomes] |
rs7040666 | 0.86[ASN][1000 genomes] |
rs7042700 | 0.92[ASN][1000 genomes] |
rs7043703 | 0.85[ASN][1000 genomes] |
rs7044254 | 0.85[ASN][1000 genomes] |
rs7044783 | 0.86[ASN][1000 genomes] |
rs7046327 | 0.86[ASN][1000 genomes] |
rs7046951 | 0.86[ASN][1000 genomes] |
rs7047093 | 0.88[ASN][1000 genomes] |
rs7848118 | 0.97[ASN][1000 genomes] |
rs7865807 | 0.88[ASN][1000 genomes] |
rs7874597 | 0.93[AFR][1000 genomes];0.99[ASN][1000 genomes] |
rs870270 | 0.95[ASN][1000 genomes] |
rs9406667 | 0.81[AFR][1000 genomes] |
rs9407792 | 0.88[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs9407793 | 0.95[ASN][1000 genomes] |
rs9407794 | 0.92[ASN][1000 genomes] |
rs9407804 | 0.96[AFR][1000 genomes];0.96[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1024799 | chr9:16631890-17431827 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
2 | esv2764141 | chr9:16903446-17351711 | Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | nsv892658 | chr9:17041557-17532840 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 11 gene(s) | inside rSNPs | diseases |
4 | nsv892661 | chr9:17134245-17532840 | Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
5 | nsv428537 | chr9:17146369-17308494 | Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv613693 | chr9:17147191-17710407 | Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
7 | nsv471287 | chr9:17165698-17708814 | Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
8 | nsv466269 | chr9:17165698-17710407 | Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
9 | nsv892662 | chr9:17168867-17329964 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
10 | nsv1031269 | chr9:17204320-17316969 | Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
11 | nsv466270 | chr9:17236376-17377629 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
12 | nsv613694 | chr9:17236376-17377629 | Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
13 | nsv892663 | chr9:17243746-17329964 | ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
14 | nsv892664 | chr9:17250170-17296630 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
15 | nsv892665 | chr9:17250170-17371690 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
16 | nsv892667 | chr9:17269437-17296630 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
17 | nsv613695 | chr9:17273731-17348412 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:17262800-17339800 | Weak transcription | Left Ventricle | heart |
2 | chr9:17273200-17301800 | Weak transcription | Dnd41 | blood |
3 | chr9:17274800-17323200 | Weak transcription | Aorta | Aorta |
4 | chr9:17281000-17300400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
5 | chr9:17284400-17309600 | Weak transcription | Ovary | ovary |
6 | chr9:17284400-17344800 | Weak transcription | Primary hematopoietic stem cells | blood |
7 | chr9:17284600-17299600 | Weak transcription | Adipose Nuclei | Adipose |
8 | chr9:17284800-17308000 | Weak transcription | Fetal Lung | lung |
9 | chr9:17285000-17311600 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
10 | chr9:17292000-17297800 | Weak transcription | HSMMtube | muscle |
11 | chr9:17292200-17367200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
12 | chr9:17292400-17303800 | Weak transcription | Right Ventricle | heart |
13 | chr9:17293600-17308600 | Weak transcription | Fetal Muscle Trunk | muscle |
14 | chr9:17293800-17314200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
15 | chr9:17294000-17295600 | Weak transcription | Stomach Smooth Muscle | stomach |
16 | chr9:17294000-17296800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
17 | chr9:17294000-17296800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
18 | chr9:17294000-17297200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
19 | chr9:17294000-17299800 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
20 | chr9:17294000-17306400 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
21 | chr9:17294000-17317600 | Weak transcription | Liver | Liver |
22 | chr9:17294000-17334000 | Weak transcription | Fetal Stomach | stomach |
23 | chr9:17294000-17346000 | Weak transcription | Fetal Muscle Leg | muscle |
24 | chr9:17294600-17311000 | Weak transcription | Primary monocytes fromperipheralblood | blood |
25 | chr9:17295400-17295600 | Enhancers | H1 Cell Line | embryonic stem cell |