Variant report
Variant | rs7929092 |
---|---|
Chromosome Location | chr11:62948985-62948986 |
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] |
---|---|
rs10750995 | 0.88[ASN][1000 genomes] |
rs10792403 | 0.88[ASN][1000 genomes] |
rs10792404 | 0.88[ASN][1000 genomes] |
rs10792406 | 0.88[ASN][1000 genomes] |
rs10897380 | 0.88[ASN][1000 genomes] |
rs10897381 | 0.88[ASN][1000 genomes] |
rs10897382 | 0.88[ASN][1000 genomes] |
rs10897383 | 0.88[ASN][1000 genomes] |
rs10897384 | 0.88[ASN][1000 genomes] |
rs10897387 | 0.80[ASN][1000 genomes] |
rs10897390 | 0.87[ASN][1000 genomes] |
rs10897392 | 0.87[ASN][1000 genomes] |
rs10897396 | 0.85[ASN][1000 genomes] |
rs10897397 | 0.85[ASN][1000 genomes] |
rs10897399 | 0.86[ASN][1000 genomes] |
rs1122524 | 0.86[ASN][1000 genomes] |
rs11231391 | 0.88[ASN][1000 genomes] |
rs11231392 | 0.88[ASN][1000 genomes] |
rs11231394 | 0.88[ASN][1000 genomes] |
rs11231395 | 0.87[ASN][1000 genomes] |
rs11231396 | 0.88[ASN][1000 genomes] |
rs11231397 | 0.88[ASN][1000 genomes] |
rs11231403 | 0.88[ASN][1000 genomes] |
rs11231409 | 0.86[ASN][1000 genomes] |
rs11231410 | 0.86[ASN][1000 genomes] |
rs11231411 | 0.86[ASN][1000 genomes] |
rs11231412 | 0.86[ASN][1000 genomes] |
rs11231413 | 0.86[ASN][1000 genomes] |
rs11231414 | 0.86[ASN][1000 genomes] |
rs11231417 | 0.85[ASN][1000 genomes] |
rs11231418 | 0.85[ASN][1000 genomes] |
rs11231419 | 0.85[ASN][1000 genomes] |
rs11494212 | 0.82[ASN][1000 genomes] |
rs11524468 | 0.87[ASN][1000 genomes] |
rs11524903 | 0.86[ASN][1000 genomes] |
rs11537206 | 0.87[ASN][1000 genomes] |
rs1193642 | 0.86[ASN][1000 genomes] |
rs1193645 | 0.86[ASN][1000 genomes] |
rs1193646 | 0.86[ASN][1000 genomes] |
rs1193733 | 0.86[ASN][1000 genomes] |
rs1193772 | 0.83[ASN][1000 genomes] |
rs1193774 | 0.83[ASN][1000 genomes] |
rs1193775 | 0.83[ASN][1000 genomes] |
rs1193856 | 0.82[ASN][1000 genomes] |
rs1193891 | 0.83[ASN][1000 genomes] |
rs1193892 | 0.86[ASN][1000 genomes] |
rs1193893 | 0.86[ASN][1000 genomes] |
rs1193894 | 0.86[ASN][1000 genomes] |
rs1193896 | 0.85[ASN][1000 genomes] |
rs1193897 | 0.83[ASN][1000 genomes] |
rs1211246 | 0.83[ASN][1000 genomes] |
rs1211550 | 0.86[ASN][1000 genomes] |
rs12224010 | 0.82[ASN][1000 genomes] |
rs12225186 | 0.83[ASN][1000 genomes] |
rs12416737 | 0.86[ASN][1000 genomes] |
rs12417255 | 0.86[ASN][1000 genomes] |
rs12417508 | 0.87[ASN][1000 genomes] |
rs12418081 | 0.86[ASN][1000 genomes] |
rs12574223 | 0.86[ASN][1000 genomes] |
rs12574967 | 0.86[ASN][1000 genomes] |
rs12576556 | 0.85[ASN][1000 genomes] |
rs12577849 | 0.85[ASN][1000 genomes] |
rs12785663 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1300795 | 0.86[ASN][1000 genomes] |
rs1300796 | 0.87[ASN][1000 genomes] |
rs1300798 | 0.87[ASN][1000 genomes] |
rs1308010 | 0.87[ASN][1000 genomes] |
rs1525064 | 0.87[ASN][1000 genomes] |
rs1525071 | 0.88[ASN][1000 genomes] |
rs1723219 | 0.86[ASN][1000 genomes] |
rs1783652 | 0.85[ASN][1000 genomes] |
rs1783654 | 0.86[ASN][1000 genomes] |
rs1830026 | 0.87[ASN][1000 genomes] |
rs1852067 | 0.87[ASN][1000 genomes] |
rs1939739 | 0.88[ASN][1000 genomes] |
rs1944091 | 0.86[ASN][1000 genomes] |
rs1997038 | 0.87[ASN][1000 genomes] |
rs2155316 | 0.88[ASN][1000 genomes] |
rs2186719 | 0.88[ASN][1000 genomes] |
rs2186721 | 0.88[ASN][1000 genomes] |
rs2222591 | 0.86[ASN][1000 genomes] |
rs2226866 | 0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2317089 | 0.88[ASN][1000 genomes] |
rs2317090 | 0.88[ASN][1000 genomes] |
rs2317093 | 0.88[ASN][1000 genomes] |
rs2510590 | 0.86[ASN][1000 genomes] |
rs2510591 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs3891629 | 0.88[ASN][1000 genomes] |
rs4000269 | 0.86[ASN][1000 genomes] |
rs4258381 | 0.87[ASN][1000 genomes] |
rs4315076 | 0.86[ASN][1000 genomes] |
rs4337047 | 0.88[ASN][1000 genomes] |
rs4344494 | 0.87[ASN][1000 genomes] |
rs4963252 | 0.88[ASN][1000 genomes] |
rs4963380 | 0.82[ASN][1000 genomes] |
rs4963381 | 0.82[ASN][1000 genomes] |
rs4963385 | 0.83[ASN][1000 genomes] |
rs55963399 | 0.85[ASN][1000 genomes] |
rs58347848 | 0.81[ASN][1000 genomes] |
rs58673340 | 0.86[ASN][1000 genomes] |
rs59019924 | 0.84[ASN][1000 genomes] |
rs59626188 | 0.86[ASN][1000 genomes] |
rs60090619 | 0.86[ASN][1000 genomes] |
rs60477987 | 0.86[ASN][1000 genomes] |
rs61928110 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61928158 | 0.86[ASN][1000 genomes] |
rs6591771 | 0.86[ASN][1000 genomes] |
rs6591778 | 0.86[ASN][1000 genomes] |
rs7115707 | 0.88[ASN][1000 genomes] |
rs7126435 | 0.85[ASN][1000 genomes] |
rs7925045 | 0.85[ASN][1000 genomes] |
rs7925760 | 0.85[ASN][1000 genomes] |
rs7928993 | 0.82[ASN][1000 genomes] |
rs7932800 | 0.85[ASN][1000 genomes] |
rs7938140 | 0.83[ASN][1000 genomes] |
rs7938146 | 0.86[ASN][1000 genomes] |
rs7938863 | 0.88[ASN][1000 genomes] |
rs7949840 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv34011 | chr11:62652779-62993702 | Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
2 | nsv1045308 | chr11:62803635-63109338 | Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv541059 | chr11:62803635-63109338 | Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
4 | nsv897626 | chr11:62839667-62967791 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
5 | nsv555177 | chr11:62847518-63110569 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
6 | nsv1049725 | chr11:62848172-63057827 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
7 | nsv541060 | chr11:62848172-63057827 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
8 | nsv1047571 | chr11:62848172-63109338 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
9 | nsv430397 | chr11:62852616-63072310 | Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
10 | esv2753282 | chr11:62883681-62986146 | Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:62939200-62952400 | Strong transcription | Liver | Liver |
2 | chr11:62946600-62949600 | Enhancers | H9 Cell Line | embryonic stem cell |
3 | chr11:62946800-62949200 | Enhancers | HUES6 Cell Line | embryonic stem cell |
4 | chr11:62946800-62949400 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
5 | chr11:62946800-62949400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
6 | chr11:62946800-62949800 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
7 | chr11:62947000-62949200 | Enhancers | HUES64 Cell Line | embryonic stem cell |
8 | chr11:62948200-62952200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
9 | chr11:62948400-62949000 | Weak transcription | H1 Cell Line | embryonic stem cell |
10 | chr11:62948400-62949800 | Enhancers | HUES48 Cell Line | embryonic stem cell |
11 | chr11:62948600-62949600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
12 | chr11:62948800-62949000 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |