Variant report
Variant | rs9489368 |
---|---|
Chromosome Location | chr6:118719645-118719646 |
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] |
---|---|
rs1016095 | 0.94[ASN][1000 genomes] |
rs10457328 | 0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10457330 | 0.80[ASN][1000 genomes] |
rs10457331 | 0.80[ASN][1000 genomes] |
rs10457334 | 0.98[ASN][1000 genomes] |
rs10457336 | 0.94[ASN][1000 genomes] |
rs10457341 | 0.89[ASN][1000 genomes] |
rs10484287 | 0.94[ASN][1000 genomes] |
rs1051429 | 0.89[ASN][1000 genomes] |
rs10872163 | 1.00[ASN][1000 genomes] |
rs11153734 | 0.80[ASN][1000 genomes] |
rs11153735 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11153737 | 1.00[ASN][1000 genomes] |
rs11153738 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11153754 | 0.94[ASN][1000 genomes] |
rs11153758 | 0.87[ASN][1000 genomes] |
rs11754973 | 0.94[ASN][1000 genomes] |
rs11756983 | 0.94[ASN][1000 genomes] |
rs12153824 | 0.83[ASN][1000 genomes] |
rs12153938 | 0.89[ASN][1000 genomes] |
rs12196194 | 0.95[ASN][1000 genomes] |
rs12204456 | 0.94[ASN][1000 genomes] |
rs12526557 | 0.85[ASN][1000 genomes] |
rs12530169 | 0.80[ASN][1000 genomes] |
rs12660455 | 0.80[ASN][1000 genomes] |
rs1344178 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1344249 | 0.98[ASN][1000 genomes] |
rs1547326 | 0.94[ASN][1000 genomes] |
rs2077161 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2157569 | 0.94[ASN][1000 genomes] |
rs2181513 | 0.87[ASN][1000 genomes] |
rs2187945 | 0.82[ASN][1000 genomes] |
rs2213858 | 0.97[ASN][1000 genomes] |
rs2356175 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2356178 | 0.84[ASN][1000 genomes] |
rs2356179 | 1.00[ASN][1000 genomes] |
rs2356180 | 1.00[ASN][1000 genomes] |
rs2356182 | 0.98[ASN][1000 genomes] |
rs2356184 | 0.83[ASN][1000 genomes] |
rs2356493 | 0.97[ASN][1000 genomes] |
rs25421 | 0.97[ASN][1000 genomes] |
rs25423 | 0.97[ASN][1000 genomes] |
rs3734382 | 0.89[ASN][1000 genomes] |
rs3951041 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3951042 | 0.80[ASN][1000 genomes] |
rs3951043 | 0.80[ASN][1000 genomes] |
rs3951044 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4027875 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4027876 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4027877 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4027878 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4027880 | 0.80[ASN][1000 genomes] |
rs4027881 | 0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4027883 | 1.00[ASN][1000 genomes] |
rs4314526 | 0.95[ASN][1000 genomes] |
rs4489189 | 0.99[ASN][1000 genomes] |
rs4502975 | 0.96[ASN][1000 genomes] |
rs4568488 | 1.00[ASN][1000 genomes] |
rs4946343 | 0.80[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs4946348 | 0.87[ASN][1000 genomes] |
rs4946349 | 0.87[ASN][1000 genomes] |
rs55868726 | 0.98[ASN][1000 genomes] |
rs57813349 | 0.80[ASN][1000 genomes] |
rs6569017 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6569021 | 0.87[ASN][1000 genomes] |
rs6569022 | 0.87[ASN][1000 genomes] |
rs6903177 | 0.85[ASN][1000 genomes] |
rs6904968 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6907846 | 0.85[ASN][1000 genomes] |
rs6919887 | 0.98[ASN][1000 genomes] |
rs6923888 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6928336 | 0.87[ASN][1000 genomes] |
rs6929390 | 0.90[ASN][1000 genomes] |
rs6930900 | 0.87[ASN][1000 genomes] |
rs6936178 | 0.80[ASN][1000 genomes] |
rs6936661 | 0.99[ASN][1000 genomes] |
rs6937642 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7740922 | 0.94[ASN][1000 genomes] |
rs7741644 | 0.94[ASN][1000 genomes] |
rs7742696 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7745692 | 0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7749208 | 0.97[ASN][1000 genomes] |
rs7749694 | 0.94[ASN][1000 genomes] |
rs7751213 | 0.87[ASN][1000 genomes] |
rs7754293 | 0.87[ASN][1000 genomes] |
rs7756973 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7757337 | 0.94[ASN][1000 genomes] |
rs7757815 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7758933 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7759088 | 0.87[ASN][1000 genomes] |
rs7761717 | 0.94[ASN][1000 genomes] |
rs7761996 | 0.97[ASN][1000 genomes] |
rs7763904 | 0.87[ASN][1000 genomes] |
rs7764093 | 0.89[EUR][1000 genomes] |
rs7766732 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7766907 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7769937 | 1.00[ASN][1000 genomes] |
rs9285429 | 0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9320650 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9320653 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9374733 | 0.81[ASN][1000 genomes] |
rs9401073 | 0.82[ASN][1000 genomes] |
rs9481790 | 0.99[ASN][1000 genomes] |
rs9481795 | 0.97[ASN][1000 genomes] |
rs9481807 | 0.98[ASN][1000 genomes] |
rs9481815 | 0.97[ASN][1000 genomes] |
rs9481819 | 0.94[ASN][1000 genomes] |
rs9481832 | 0.87[ASN][1000 genomes] |
rs9489373 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9489376 | 1.00[ASN][1000 genomes] |
rs9489377 | 1.00[ASN][1000 genomes] |
rs9489378 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9489401 | 0.98[ASN][1000 genomes] |
rs9489403 | 0.98[ASN][1000 genomes] |
rs9489406 | 0.97[ASN][1000 genomes] |
rs9489414 | 0.97[ASN][1000 genomes] |
rs9489417 | 0.95[ASN][1000 genomes] |
rs9489419 | 0.94[ASN][1000 genomes] |
rs9489420 | 0.94[ASN][1000 genomes] |
rs9489421 | 0.92[ASN][1000 genomes] |
rs9489424 | 0.94[ASN][1000 genomes] |
rs9489425 | 0.94[ASN][1000 genomes] |
rs9489432 | 0.90[ASN][1000 genomes] |
rs9489437 | 0.89[ASN][1000 genomes] |
rs9489438 | 0.89[ASN][1000 genomes] |
rs9489439 | 0.89[ASN][1000 genomes] |
rs9489446 | 0.82[ASN][1000 genomes] |
rs9489448 | 0.87[ASN][1000 genomes] |
rs9489449 | 0.87[ASN][1000 genomes] |
rs9489454 | 0.87[ASN][1000 genomes] |
rs9489455 | 0.87[ASN][1000 genomes] |
rs9489456 | 0.87[ASN][1000 genomes] |
rs9489459 | 0.89[ASN][1000 genomes] |
rs9717286 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532051 | chr6:118551027-119044197 | Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1020463 | chr6:118593028-119146363 | Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
3 | nsv830787 | chr6:118631902-118805106 | Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1025403 | chr6:118635123-119122551 | Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
5 | nsv1025456 | chr6:118669672-119058789 | Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
6 | nsv1027444 | chr6:118687556-119121660 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
7 | nsv538428 | chr6:118687556-119121660 | Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
8 | nsv949321 | chr6:118692304-119137658 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
9 | nsv432958 | chr6:118692307-119010307 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
10 | nsv604555 | chr6:118695049-118856822 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
11 | nsv1034448 | chr6:118698169-119016383 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
12 | nsv1025097 | chr6:118699752-119058789 | Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
13 | nsv1020586 | chr6:118711098-118900012 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
14 | nsv532052 | chr6:118711850-119057295 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
15 | nsv432959 | chr6:118716318-119010307 | Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:118707400-118729200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr6:118711200-118729000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
3 | chr6:118712000-118727800 | Weak transcription | Primary T cells from cord blood | blood |
4 | chr6:118715800-118731800 | Weak transcription | Pancreas | Pancrea |
5 | chr6:118717400-118721800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
6 | chr6:118718600-118720000 | Enhancers | Fetal Heart | heart |
7 | chr6:118718600-118720000 | Enhancers | Fetal Muscle Leg | muscle |
8 | chr6:118718600-118720200 | Enhancers | HSMMtube | muscle |
9 | chr6:118719000-118722400 | Weak transcription | Left Ventricle | heart |
10 | chr6:118719000-118722400 | Weak transcription | Psoas Muscle | Psoas |
11 | chr6:118719200-118719800 | Weak transcription | Aorta | Aorta |
12 | chr6:118719400-118719800 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
13 | chr6:118719400-118721800 | Enhancers | Skeletal Muscle Male | skeletal muscle |