Variant report
Variant | rs11740598 |
---|---|
Chromosome Location | chr5:96188361-96188362 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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rs_ID | r2[population] |
---|---|
rs10515246 | 1.00[AFR][1000 genomes] |
rs10515247 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs10515248 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs10515249 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs10515250 | 1.00[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs11135480 | 1.00[AFR][1000 genomes] |
rs11738115 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11738810 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs11739020 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11740375 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11741100 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11742261 | 1.00[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs11743410 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs11746534 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs11747148 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11747179 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11747896 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11748328 | 1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11748519 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs11748795 | 1.00[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs11749811 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs11750464 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs11750671 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11750934 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs12186366 | 1.00[AFR][1000 genomes] |
rs13601 | 1.00[AFR][1000 genomes] |
rs17401901 | 1.00[AFR][1000 genomes] |
rs17402639 | 1.00[AFR][1000 genomes] |
rs17402704 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs17405676 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs17481334 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs17481759 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs17481856 | 1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs17484359 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2042386 | 1.00[AFR][1000 genomes];0.94[EUR][1000 genomes] |
rs3333 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs3334 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs3335 | 1.00[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs35898772 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs55773007 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs55996659 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs56119802 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs56319744 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs56395748 | 1.00[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs72773905 | 1.00[AFR][1000 genomes] |
rs72773906 | 1.00[AFR][1000 genomes] |
rs72773912 | 1.00[AFR][1000 genomes] |
rs72773917 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs72773922 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs72773923 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs72773932 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs72773942 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs72773947 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72773950 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72773968 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs72773969 | 1.00[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs72773981 | 1.00[AFR][1000 genomes];0.94[EUR][1000 genomes] |
rs72773986 | 1.00[AFR][1000 genomes];0.94[EUR][1000 genomes] |
rs72773989 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72773991 | 1.00[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs72775807 | 1.00[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs72775809 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs72775817 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72775818 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv432755 | chr5:95987984-96657483 | Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 66 gene(s) | inside rSNPs | diseases |
2 | nsv598962 | chr5:96057891-96893164 | Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
3 | nsv516293 | chr5:96070205-96216387 | Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
4 | nsv948703 | chr5:96078309-96368839 | Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 32 gene(s) | inside rSNPs | diseases |
5 | nsv1027472 | chr5:96081592-96337550 | Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
6 | nsv1028741 | chr5:96082401-96372165 | Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 32 gene(s) | inside rSNPs | diseases |
7 | nsv949058 | chr5:96082433-96390619 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
8 | nsv598963 | chr5:96084776-96363407 | Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
9 | nsv432756 | chr5:96113844-96234644 | Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
10 | nsv531967 | chr5:96127842-96302702 | Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:96186800-96188800 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
2 | chr5:96187000-96190800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr5:96187200-96190200 | Enhancers | NHDF-Ad | bronchial |
4 | chr5:96187400-96188400 | Weak transcription | Osteobl | bone |
5 | chr5:96187400-96190200 | Weak transcription | NHLF | lung |
6 | chr5:96187800-96188800 | Weak transcription | Adipose Nuclei | Adipose |
7 | chr5:96188000-96188400 | Enhancers | Fetal Brain Male | brain |
8 | chr5:96188000-96189000 | Enhancers | NH-A | brain |
9 | chr5:96188200-96189200 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |