Variant report
| Variant | rs73408259 |
|---|---|
| Chromosome Location | chr7:102590076-102590077 |
| allele | G/T |
| Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr7:102589644..102592537-chr7:102602943..102605917,2 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
| rs_ID | r2[population] |
|---|---|
| rs10229137 | 1.00[EUR][1000 genomes] |
| rs10230292 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs10230700 | 1.00[AMR][1000 genomes] |
| rs10240546 | 1.00[EUR][1000 genomes] |
| rs10260344 | 1.00[EUR][1000 genomes] |
| rs10264869 | 1.00[EUR][1000 genomes] |
| rs10268849 | 1.00[EUR][1000 genomes] |
| rs10808123 | 1.00[EUR][1000 genomes] |
| rs10808124 | 1.00[EUR][1000 genomes] |
| rs10808125 | 1.00[EUR][1000 genomes] |
| rs10808127 | 1.00[EUR][1000 genomes] |
| rs11560367 | 1.00[EUR][1000 genomes] |
| rs11760826 | 1.00[EUR][1000 genomes] |
| rs11765948 | 1.00[EUR][1000 genomes] |
| rs11772979 | 1.00[EUR][1000 genomes] |
| rs11773883 | 1.00[EUR][1000 genomes] |
| rs11981558 | 1.00[EUR][1000 genomes] |
| rs12155099 | 1.00[EUR][1000 genomes] |
| rs12539639 | 1.00[EUR][1000 genomes] |
| rs13225565 | 1.00[EUR][1000 genomes] |
| rs13226097 | 1.00[EUR][1000 genomes] |
| rs13242079 | 1.00[EUR][1000 genomes] |
| rs13247932 | 1.00[EUR][1000 genomes] |
| rs1404213 | 1.00[EUR][1000 genomes] |
| rs1477159 | 1.00[EUR][1000 genomes] |
| rs1477161 | 1.00[EUR][1000 genomes] |
| rs1477162 | 1.00[EUR][1000 genomes] |
| rs1477163 | 1.00[EUR][1000 genomes] |
| rs1558853 | 1.00[EUR][1000 genomes] |
| rs1861725 | 1.00[EUR][1000 genomes] |
| rs1861726 | 1.00[EUR][1000 genomes] |
| rs1861728 | 1.00[EUR][1000 genomes] |
| rs1861730 | 1.00[EUR][1000 genomes] |
| rs1861732 | 1.00[EUR][1000 genomes] |
| rs1968198 | 1.00[EUR][1000 genomes] |
| rs1968199 | 1.00[EUR][1000 genomes] |
| rs1968202 | 1.00[EUR][1000 genomes] |
| rs1974715 | 1.00[EUR][1000 genomes] |
| rs1974716 | 1.00[EUR][1000 genomes] |
| rs2015289 | 1.00[EUR][1000 genomes] |
| rs2041949 | 1.00[EUR][1000 genomes] |
| rs2098447 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2111381 | 1.00[EUR][1000 genomes] |
| rs2193418 | 1.00[EUR][1000 genomes] |
| rs2411079 | 1.00[EUR][1000 genomes] |
| rs2411081 | 1.00[EUR][1000 genomes] |
| rs2411082 | 1.00[EUR][1000 genomes] |
| rs2898640 | 1.00[EUR][1000 genomes] |
| rs3181009 | 1.00[EUR][1000 genomes] |
| rs4295594 | 1.00[EUR][1000 genomes] |
| rs4530973 | 1.00[EUR][1000 genomes] |
| rs4727560 | 1.00[EUR][1000 genomes] |
| rs4727561 | 1.00[EUR][1000 genomes] |
| rs4729868 | 1.00[EUR][1000 genomes] |
| rs4729869 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs4729870 | 1.00[EUR][1000 genomes] |
| rs4729871 | 1.00[EUR][1000 genomes] |
| rs4729872 | 1.00[EUR][1000 genomes] |
| rs4729875 | 1.00[EUR][1000 genomes] |
| rs4729876 | 1.00[EUR][1000 genomes] |
| rs4729878 | 1.00[EUR][1000 genomes] |
| rs4729882 | 1.00[EUR][1000 genomes] |
| rs4729883 | 1.00[EUR][1000 genomes] |
| rs4729884 | 1.00[EUR][1000 genomes] |
| rs56938507 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs57013410 | 1.00[EUR][1000 genomes] |
| rs57055721 | 1.00[EUR][1000 genomes] |
| rs61187383 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs61676871 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6465891 | 1.00[EUR][1000 genomes] |
| rs6465892 | 1.00[EUR][1000 genomes] |
| rs6465898 | 1.00[EUR][1000 genomes] |
| rs6465902 | 1.00[EUR][1000 genomes] |
| rs6465905 | 1.00[EUR][1000 genomes] |
| rs6465907 | 1.00[EUR][1000 genomes] |
| rs6944809 | 1.00[EUR][1000 genomes] |
| rs6945578 | 1.00[EUR][1000 genomes] |
| rs6946968 | 1.00[EUR][1000 genomes] |
| rs6946989 | 1.00[EUR][1000 genomes] |
| rs6947777 | 1.00[EUR][1000 genomes] |
| rs6950177 | 1.00[EUR][1000 genomes] |
| rs6955436 | 1.00[EUR][1000 genomes] |
| rs6959711 | 1.00[EUR][1000 genomes] |
| rs6964822 | 1.00[EUR][1000 genomes] |
| rs6966872 | 1.00[EUR][1000 genomes] |
| rs6966961 | 1.00[EUR][1000 genomes] |
| rs6968559 | 0.88[AFR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6973702 | 1.00[EUR][1000 genomes] |
| rs6973787 | 1.00[EUR][1000 genomes] |
| rs6976034 | 1.00[EUR][1000 genomes] |
| rs6976290 | 1.00[EUR][1000 genomes] |
| rs6976794 | 1.00[EUR][1000 genomes] |
| rs6977206 | 1.00[EUR][1000 genomes] |
| rs6979140 | 1.00[EUR][1000 genomes] |
| rs6979470 | 1.00[EUR][1000 genomes] |
| rs73406252 | 1.00[EUR][1000 genomes] |
| rs73408205 | 1.00[EUR][1000 genomes] |
| rs73408207 | 1.00[EUR][1000 genomes] |
| rs73408209 | 0.88[AFR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73408210 | 1.00[EUR][1000 genomes] |
| rs73408223 | 1.00[EUR][1000 genomes] |
| rs73408251 | 1.00[EUR][1000 genomes] |
| rs73408254 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73408255 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73408285 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73408286 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73410119 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73410129 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs73410143 | 1.00[EUR][1000 genomes] |
| rs7349957 | 1.00[EUR][1000 genomes] |
| rs7350051 | 1.00[EUR][1000 genomes] |
| rs7782147 | 1.00[EUR][1000 genomes] |
| rs7783856 | 1.00[EUR][1000 genomes] |
| rs7784337 | 1.00[EUR][1000 genomes] |
| rs7792240 | 1.00[EUR][1000 genomes] |
| rs7800789 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs7807900 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs9640672 | 1.00[EUR][1000 genomes] |
| rs9641307 | 1.00[EUR][1000 genomes] |
| rs9641308 | 1.00[EUR][1000 genomes] |
| rs9691829 | 1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1016563 | chr7:101912320-102695860 | Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 76 gene(s) | inside rSNPs | diseases |
| 2 | nsv1028438 | chr7:101912320-102704135 | Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 76 gene(s) | inside rSNPs | diseases |
| 3 | nsv868996 | chr7:102332827-102991361 | ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS 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 | 46 gene(s) | inside rSNPs | diseases |
| 4 | esv2752138 | chr7:102358320-102787135 | Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
| 5 | nsv464667 | chr7:102486254-102624192 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
| 6 | nsv608060 | chr7:102486254-102624192 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:102573800-102591400 | Weak transcription | Pancreas | Pancrea |
| 2 | chr7:102574000-102592200 | Weak transcription | Fetal Intestine Large | intestine |
| 3 | chr7:102574600-102594400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 4 | chr7:102582800-102590800 | Weak transcription | Fetal Stomach | stomach |
| 5 | chr7:102587000-102590400 | Weak transcription | Fetal Lung | lung |
| 6 | chr7:102587000-102590800 | Weak transcription | HSMMtube | muscle |
| 7 | chr7:102588000-102590200 | Weak transcription | K562 | blood |
| 8 | chr7:102589400-102591000 | Strong transcription | HSMM | muscle |





