Variant report
Variant | rs1560743 |
---|---|
Chromosome Location | chr12:73016980-73016981 |
allele | A/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] |
---|---|
rs10128837 | 0.81[ASN][1000 genomes] |
rs10128853 | 0.80[ASN][1000 genomes] |
rs10128854 | 0.80[ASN][1000 genomes] |
rs10129051 | 0.81[ASN][1000 genomes] |
rs1017987 | 0.84[ASN][1000 genomes] |
rs1032330 | 0.80[ASN][1000 genomes] |
rs1032331 | 0.80[ASN][1000 genomes] |
rs1032332 | 0.81[ASN][1000 genomes] |
rs10506656 | 0.80[ASN][1000 genomes] |
rs10506657 | 0.81[ASN][1000 genomes] |
rs10506658 | 0.81[ASN][1000 genomes] |
rs10748199 | 0.80[ASN][1000 genomes] |
rs10784971 | 0.80[ASN][1000 genomes] |
rs10784972 | 0.80[ASN][1000 genomes] |
rs10784973 | 0.81[ASN][1000 genomes] |
rs10879444 | 0.81[ASN][1000 genomes] |
rs10879445 | 0.81[ASN][1000 genomes] |
rs10879446 | 0.80[ASN][1000 genomes] |
rs10879447 | 0.80[ASN][1000 genomes] |
rs10879451 | 0.84[ASN][1000 genomes] |
rs10879453 | 0.83[ASN][1000 genomes] |
rs10879458 | 0.86[ASN][1000 genomes] |
rs10879459 | 0.87[ASN][1000 genomes] |
rs10879460 | 0.90[ASN][1000 genomes] |
rs10879465 | 0.81[ASN][1000 genomes] |
rs10879466 | 0.81[ASN][1000 genomes] |
rs10879472 | 0.85[ASN][1000 genomes] |
rs10879473 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11179253 | 0.81[ASN][1000 genomes] |
rs11179255 | 0.81[ASN][1000 genomes] |
rs11179256 | 0.81[ASN][1000 genomes] |
rs11179258 | 0.81[ASN][1000 genomes] |
rs11179259 | 0.81[ASN][1000 genomes] |
rs11179261 | 0.84[ASN][1000 genomes] |
rs11179264 | 0.85[ASN][1000 genomes] |
rs11179267 | 0.84[ASN][1000 genomes] |
rs11179288 | 0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11179289 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11179290 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11179293 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11179294 | 0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs11179295 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11179296 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs11179298 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11179302 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11179307 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11179308 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11179309 | 0.97[ASN][1000 genomes] |
rs11610020 | 0.99[ASN][1000 genomes] |
rs11613768 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11832310 | 0.84[ASN][1000 genomes] |
rs11833556 | 0.83[ASN][1000 genomes] |
rs11834716 | 0.84[ASN][1000 genomes] |
rs11836997 | 0.84[ASN][1000 genomes] |
rs12099552 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12296996 | 0.81[ASN][1000 genomes] |
rs12297086 | 0.81[ASN][1000 genomes] |
rs12297782 | 0.81[ASN][1000 genomes] |
rs12298218 | 0.85[ASN][1000 genomes] |
rs12298495 | 0.84[ASN][1000 genomes] |
rs12298959 | 0.81[ASN][1000 genomes] |
rs12302064 | 0.81[ASN][1000 genomes] |
rs12302437 | 0.84[ASN][1000 genomes] |
rs12302523 | 0.81[ASN][1000 genomes] |
rs12304007 | 0.81[ASN][1000 genomes] |
rs12304367 | 0.81[ASN][1000 genomes] |
rs12310334 | 0.81[ASN][1000 genomes] |
rs12310446 | 0.81[ASN][1000 genomes] |
rs12310724 | 0.81[ASN][1000 genomes] |
rs12322419 | 0.81[ASN][1000 genomes] |
rs12581283 | 0.84[ASN][1000 genomes] |
rs12582138 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12816288 | 0.85[ASN][1000 genomes] |
rs12824763 | 0.84[ASN][1000 genomes] |
rs12824967 | 0.84[ASN][1000 genomes] |
rs1463756 | 0.80[ASN][1000 genomes] |
rs1469721 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1560742 | 1.00[ASN][1000 genomes] |
rs17111389 | 0.80[ASN][1000 genomes] |
rs17111470 | 0.81[ASN][1000 genomes] |
rs1826590 | 0.81[ASN][1000 genomes] |
rs1826591 | 0.80[ASN][1000 genomes] |
rs1844642 | 0.81[ASN][1000 genomes] |
rs1873347 | 0.84[ASN][1000 genomes] |
rs1873348 | 0.80[ASN][1000 genomes] |
rs1907087 | 0.81[ASN][1000 genomes] |
rs1908180 | 0.81[ASN][1000 genomes] |
rs1962706 | 0.83[ASN][1000 genomes] |
rs1968964 | 0.80[ASN][1000 genomes] |
rs1968965 | 0.81[ASN][1000 genomes] |
rs1991751 | 0.81[ASN][1000 genomes] |
rs2272503 | 0.81[ASN][1000 genomes] |
rs2272504 | 0.80[ASN][1000 genomes] |
rs2272505 | 0.80[ASN][1000 genomes] |
rs2272506 | 0.81[ASN][1000 genomes] |
rs2272507 | 0.80[ASN][1000 genomes] |
rs2367746 | 0.81[ASN][1000 genomes] |
rs2367748 | 0.83[ASN][1000 genomes] |
rs2367750 | 0.81[ASN][1000 genomes] |
rs305396 | 0.85[ASN][1000 genomes] |
rs34115559 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs34893785 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs35902343 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3782368 | 0.81[ASN][1000 genomes] |
rs3817611 | 0.81[ASN][1000 genomes] |
rs3858591 | 0.80[ASN][1000 genomes] |
rs3936356 | 0.99[ASN][1000 genomes] |
rs3952786 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs41387445 | 0.90[ASN][1000 genomes] |
rs4144975 | 0.84[ASN][1000 genomes] |
rs458942 | 0.82[ASN][1000 genomes] |
rs460406 | 0.85[ASN][1000 genomes] |
rs57810138 | 0.81[ASN][1000 genomes] |
rs58509346 | 0.87[ASN][1000 genomes] |
rs58687032 | 0.87[ASN][1000 genomes] |
rs6582093 | 0.88[ASN][1000 genomes] |
rs66495167 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs68011183 | 0.81[ASN][1000 genomes] |
rs7139104 | 0.81[ASN][1000 genomes] |
rs7296349 | 0.84[ASN][1000 genomes] |
rs7296979 | 0.80[ASN][1000 genomes] |
rs7297703 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7298834 | 0.84[ASN][1000 genomes] |
rs7299196 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7303841 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7315299 | 0.84[ASN][1000 genomes] |
rs7315407 | 0.84[ASN][1000 genomes] |
rs7955512 | 0.81[ASN][1000 genomes] |
rs7955675 | 0.81[ASN][1000 genomes] |
rs7955871 | 0.80[ASN][1000 genomes] |
rs7970163 | 0.81[ASN][1000 genomes] |
rs9705508 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs972421 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2422452 | chr12:72485933-73175581 | Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
2 | nsv899257 | chr12:72569746-73145896 | ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
3 | nsv1044083 | chr12:72647640-73275526 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
4 | nsv469465 | chr12:72655925-73259114 | Weak transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
5 | nsv559363 | chr12:72655925-73259114 | Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
6 | nsv868884 | chr12:72664763-73241518 | Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
7 | nsv817280 | chr12:72820558-73508605 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
8 | nsv832454 | chr12:72940798-73081180 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv1054725 | chr12:72990553-73062598 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
10 | esv2758314 | chr12:72990707-73251109 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
11 | esv2759908 | chr12:72990707-73251109 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
12 | nsv868885 | chr12:72998553-73587081 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:73005000-73051600 | Weak transcription | Fetal Intestine Large | intestine |
2 | chr12:73005200-73038000 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
3 | chr12:73005200-73053200 | Weak transcription | Ovary | ovary |
4 | chr12:73011400-73059000 | Weak transcription | Pancreas | Pancrea |
5 | chr12:73014400-73042000 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
6 | chr12:73014800-73055800 | Weak transcription | Adipose Nuclei | Adipose |
7 | chr12:73015200-73017600 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
8 | chr12:73015200-73019000 | Weak transcription | Fetal Intestine Small | intestine |
9 | chr12:73016800-73017200 | Weak transcription | Liver | Liver |