Variant report
Variant | rs1193772 |
---|---|
Chromosome Location | chr11:63018909-63018910 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:1 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-SLC22A9-2 | chr11:63018729-63019657 | l_487_chr11:63018728-63024659_testes |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10750995 | 0.94[ASN][1000 genomes] |
rs10792403 | 0.94[ASN][1000 genomes] |
rs10792404 | 0.94[ASN][1000 genomes] |
rs10792406 | 0.94[ASN][1000 genomes] |
rs10897380 | 0.94[ASN][1000 genomes] |
rs10897381 | 0.94[ASN][1000 genomes] |
rs10897382 | 0.94[ASN][1000 genomes] |
rs10897383 | 0.94[ASN][1000 genomes] |
rs10897384 | 0.94[ASN][1000 genomes] |
rs10897387 | 0.90[ASN][1000 genomes] |
rs10897390 | 0.96[ASN][1000 genomes] |
rs10897392 | 0.96[ASN][1000 genomes] |
rs10897396 | 0.96[ASN][1000 genomes] |
rs10897397 | 0.96[ASN][1000 genomes] |
rs10897399 | 0.87[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs1122524 | 0.90[ASN][1000 genomes] |
rs11231391 | 0.94[ASN][1000 genomes] |
rs11231392 | 0.94[ASN][1000 genomes] |
rs11231394 | 0.94[ASN][1000 genomes] |
rs11231395 | 0.93[ASN][1000 genomes] |
rs11231396 | 0.94[ASN][1000 genomes] |
rs11231397 | 0.94[ASN][1000 genomes] |
rs11231403 | 0.94[ASN][1000 genomes] |
rs11231406 | 0.83[ASN][1000 genomes] |
rs11231409 | 0.97[ASN][1000 genomes] |
rs11231410 | 0.97[ASN][1000 genomes] |
rs11231411 | 0.97[ASN][1000 genomes] |
rs11231412 | 0.97[ASN][1000 genomes] |
rs11231413 | 0.97[ASN][1000 genomes] |
rs11231414 | 0.97[ASN][1000 genomes] |
rs11231417 | 0.96[ASN][1000 genomes] |
rs11231418 | 0.96[ASN][1000 genomes] |
rs11231419 | 0.96[ASN][1000 genomes] |
rs11494212 | 0.91[ASN][1000 genomes] |
rs1152244 | 0.89[ASN][1000 genomes] |
rs1152245 | 0.90[ASN][1000 genomes] |
rs1152246 | 0.90[ASN][1000 genomes] |
rs11524468 | 0.82[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs11524903 | 0.97[ASN][1000 genomes] |
rs11537206 | 0.93[ASN][1000 genomes] |
rs11559570 | 0.86[ASN][1000 genomes] |
rs1193642 | 0.97[ASN][1000 genomes] |
rs1193645 | 0.97[ASN][1000 genomes] |
rs1193646 | 0.97[ASN][1000 genomes] |
rs1193718 | 0.91[ASN][1000 genomes] |
rs1193726 | 0.90[ASN][1000 genomes] |
rs1193729 | 0.89[ASN][1000 genomes] |
rs1193733 | 0.97[ASN][1000 genomes] |
rs1193774 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1193775 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1193789 | 0.90[ASN][1000 genomes] |
rs1193856 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1193891 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1193892 | 0.97[ASN][1000 genomes] |
rs1193893 | 0.97[ASN][1000 genomes] |
rs1193894 | 0.97[ASN][1000 genomes] |
rs1193896 | 0.96[ASN][1000 genomes] |
rs1193897 | 0.94[ASN][1000 genomes] |
rs1193904 | 0.82[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs1193905 | 0.90[ASN][1000 genomes] |
rs1201559 | 0.91[ASN][1000 genomes] |
rs1205166 | 0.90[ASN][1000 genomes] |
rs1205186 | 0.90[ASN][1000 genomes] |
rs1211246 | 0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1211550 | 0.95[ASN][1000 genomes] |
rs12224010 | 0.94[ASN][1000 genomes] |
rs12225186 | 0.94[ASN][1000 genomes] |
rs12416737 | 0.97[ASN][1000 genomes] |
rs12417255 | 0.97[ASN][1000 genomes] |
rs12417508 | 0.96[ASN][1000 genomes] |
rs12418081 | 0.97[ASN][1000 genomes] |
rs12574223 | 0.97[ASN][1000 genomes] |
rs12574967 | 0.97[ASN][1000 genomes] |
rs12576556 | 0.96[ASN][1000 genomes] |
rs12577849 | 0.96[ASN][1000 genomes] |
rs1300795 | 0.97[ASN][1000 genomes] |
rs1300796 | 0.96[ASN][1000 genomes] |
rs1300798 | 0.96[ASN][1000 genomes] |
rs1308010 | 0.96[ASN][1000 genomes] |
rs1404608 | 0.91[ASN][1000 genomes] |
rs1525064 | 0.96[ASN][1000 genomes] |
rs1525071 | 0.94[ASN][1000 genomes] |
rs1608760 | 0.90[ASN][1000 genomes] |
rs1723213 | 0.91[ASN][1000 genomes] |
rs1723219 | 0.97[ASN][1000 genomes] |
rs1783634 | 0.91[ASN][1000 genomes] |
rs1783652 | 0.96[ASN][1000 genomes] |
rs1783654 | 0.97[ASN][1000 genomes] |
rs1789327 | 0.89[ASN][1000 genomes] |
rs1789334 | 0.91[ASN][1000 genomes] |
rs1790218 | 0.90[ASN][1000 genomes] |
rs1830026 | 0.96[ASN][1000 genomes] |
rs1852067 | 0.96[ASN][1000 genomes] |
rs1939739 | 0.94[ASN][1000 genomes] |
rs1944091 | 0.97[ASN][1000 genomes] |
rs1944092 | 0.82[ASN][1000 genomes] |
rs1997038 | 0.96[ASN][1000 genomes] |
rs2155316 | 0.94[ASN][1000 genomes] |
rs2186719 | 0.94[ASN][1000 genomes] |
rs2186721 | 0.94[ASN][1000 genomes] |
rs2222591 | 0.94[ASN][1000 genomes] |
rs2226866 | 0.82[ASN][1000 genomes] |
rs2317089 | 0.94[ASN][1000 genomes] |
rs2317090 | 0.94[ASN][1000 genomes] |
rs2317093 | 0.94[ASN][1000 genomes] |
rs2510590 | 0.97[ASN][1000 genomes] |
rs2510591 | 0.82[ASN][1000 genomes] |
rs3891629 | 0.94[ASN][1000 genomes] |
rs3915142 | 0.91[ASN][1000 genomes] |
rs3937020 | 0.90[ASN][1000 genomes] |
rs4000269 | 0.82[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs4060975 | 0.85[ASN][1000 genomes] |
rs4258381 | 0.96[ASN][1000 genomes] |
rs4315076 | 0.97[ASN][1000 genomes] |
rs4337047 | 0.94[ASN][1000 genomes] |
rs4344494 | 0.96[ASN][1000 genomes] |
rs4445638 | 0.90[ASN][1000 genomes] |
rs474096 | 0.91[ASN][1000 genomes] |
rs474191 | 0.91[ASN][1000 genomes] |
rs474815 | 0.87[ASN][1000 genomes] |
rs474874 | 0.91[ASN][1000 genomes] |
rs483012 | 0.91[ASN][1000 genomes] |
rs486460 | 0.90[ASN][1000 genomes] |
rs4963252 | 0.94[ASN][1000 genomes] |
rs4963380 | 0.88[ASN][1000 genomes] |
rs4963381 | 0.88[ASN][1000 genomes] |
rs4963385 | 0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs505653 | 0.91[ASN][1000 genomes] |
rs513338 | 0.91[ASN][1000 genomes] |
rs515213 | 0.91[ASN][1000 genomes] |
rs524724 | 0.91[ASN][1000 genomes] |
rs527027 | 0.80[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs527869 | 0.90[ASN][1000 genomes] |
rs532085 | 0.91[ASN][1000 genomes] |
rs534799 | 0.91[ASN][1000 genomes] |
rs537194 | 0.82[ASN][1000 genomes] |
rs540141 | 0.90[ASN][1000 genomes] |
rs543429 | 0.90[ASN][1000 genomes] |
rs548885 | 0.91[ASN][1000 genomes] |
rs549144 | 0.88[ASN][1000 genomes] |
rs554430 | 0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs557658 | 0.91[ASN][1000 genomes] |
rs557879 | 0.91[ASN][1000 genomes] |
rs55963399 | 0.94[ASN][1000 genomes] |
rs56030503 | 0.89[ASN][1000 genomes] |
rs565787 | 0.91[ASN][1000 genomes] |
rs572017 | 0.91[ASN][1000 genomes] |
rs575009 | 0.91[ASN][1000 genomes] |
rs576641 | 0.91[ASN][1000 genomes] |
rs58347848 | 0.92[ASN][1000 genomes] |
rs58673340 | 0.97[ASN][1000 genomes] |
rs59019924 | 0.89[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs59626188 | 0.97[ASN][1000 genomes] |
rs60090619 | 0.85[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs60477987 | 0.97[ASN][1000 genomes] |
rs61928110 | 0.83[ASN][1000 genomes] |
rs61928158 | 0.97[ASN][1000 genomes] |
rs6591771 | 0.90[ASN][1000 genomes] |
rs6591772 | 0.87[ASN][1000 genomes] |
rs6591778 | 0.97[ASN][1000 genomes] |
rs7115707 | 0.94[ASN][1000 genomes] |
rs7126435 | 0.96[ASN][1000 genomes] |
rs7130728 | 0.91[ASN][1000 genomes] |
rs7925045 | 0.94[ASN][1000 genomes] |
rs7925760 | 0.93[ASN][1000 genomes] |
rs7928993 | 0.88[ASN][1000 genomes] |
rs7929092 | 0.83[ASN][1000 genomes] |
rs7932800 | 0.96[ASN][1000 genomes] |
rs7938140 | 1.00[ASN][1000 genomes] |
rs7938146 | 0.97[ASN][1000 genomes] |
rs7938863 | 0.94[ASN][1000 genomes] |
rs7949840 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | 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 |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
8 | nsv897627 | chr11:62984868-63119486 | Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
9 | nsv1051171 | chr11:62987064-63835715 | Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 100 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:63008800-63021800 | Enhancers | HepG2 | liver |
2 | chr11:63018800-63020600 | Enhancers | Liver | Liver |