Variant report
Variant | rs646117 |
---|---|
Chromosome Location | chr4:1091829-1091830 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000251639 | Chromatin interaction |
ENSG00000178222 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10032349 | 0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs10032470 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs10033163 | 0.97[EUR][1000 genomes] |
rs11724989 | 0.86[EUR][1000 genomes] |
rs11728360 | 0.80[EUR][1000 genomes] |
rs11732259 | 0.83[EUR][1000 genomes] |
rs11736950 | 0.83[EUR][1000 genomes] |
rs13119696 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs13146371 | 0.82[AFR][1000 genomes] |
rs1383660 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1481167 | 0.83[EUR][1000 genomes] |
rs1680027 | 0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1825092 | 0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs28374671 | 0.86[EUR][1000 genomes] |
rs28510738 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs28514301 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs28579427 | 0.83[EUR][1000 genomes] |
rs28588234 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2924495 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4246683 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4246684 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4974561 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4974569 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4974571 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4974628 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4974637 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4974639 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4974642 | 0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4974643 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4974644 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs55741287 | 0.82[AFR][1000 genomes] |
rs583100 | 0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs584472 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs588824 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs589660 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59057706 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs604526 | 0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs606293 | 0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs606327 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs608066 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs614945 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs615381 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs616196 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs616569 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs617633 | 0.86[EUR][1000 genomes] |
rs619407 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs620398 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs629638 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs630549 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs632319 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs633087 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs633141 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs633599 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs633954 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs636976 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs643043 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs647828 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs648640 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs649243 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs649258 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs649616 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs649950 | 0.98[AFR][1000 genomes];0.86[AMR][1000 genomes] |
rs651135 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs651509 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs658320 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6599282 | 0.80[EUR][1000 genomes] |
rs6599283 | 0.83[EUR][1000 genomes] |
rs661364 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs671790 | 0.84[EUR][1000 genomes] |
rs674347 | 0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6814094 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6814276 | 0.86[EUR][1000 genomes] |
rs6817989 | 0.86[EUR][1000 genomes] |
rs681857 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs682243 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs682787 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6839768 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs6840162 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6852246 | 0.85[EUR][1000 genomes] |
rs687939 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs689216 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs73074169 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7686839 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7691553 | 0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9992322 | 0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv822425 | chr4:540105-1413799 | Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 108 gene(s) | inside rSNPs | diseases |
2 | nsv530490 | chr4:614355-1399150 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 104 gene(s) | inside rSNPs | diseases |
3 | nsv1003219 | chr4:769894-1105464 | Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 45 gene(s) | inside rSNPs | diseases |
4 | nsv536980 | chr4:827866-1167377 | Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
5 | nsv1009619 | chr4:901897-1215657 | Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
6 | nsv1003876 | chr4:927509-1191316 | Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
7 | nsv1000381 | chr4:927509-1198766 | Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
8 | esv3339080 | chr4:970630-1546223 | Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 82 gene(s) | inside rSNPs | diseases |
9 | nsv1004727 | chr4:1015652-1158207 | Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
10 | nsv536984 | chr4:1015652-1158207 | Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
11 | nsv1005990 | chr4:1015652-1167619 | Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
12 | nsv1000594 | chr4:1045099-1129975 | Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
13 | nsv1001165 | chr4:1051512-1129975 | Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
14 | nsv1012892 | chr4:1086871-1176630 | Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
15 | esv3355565 | chr4:1087452-1092050 | Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:1084200-1093400 | Weak transcription | Ovary | ovary |
2 | chr4:1086000-1098400 | Weak transcription | Lung | lung |
3 | chr4:1086200-1098600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
4 | chr4:1088400-1093400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr4:1088600-1093600 | Weak transcription | Fetal Muscle Trunk | muscle |
6 | chr4:1090400-1093400 | Enhancers | Pancreas | Pancrea |