Variant report
Variant | rs28742222 |
---|---|
Chromosome Location | chr7:40176752-40176753 |
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] |
---|---|
rs10081308 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10081355 | 0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10156182 | 0.89[EUR][1000 genomes] |
rs10227386 | 0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10228020 | 0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10229517 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10230530 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10234693 | 0.89[EUR][1000 genomes] |
rs10242519 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10243494 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10246466 | 0.89[EUR][1000 genomes] |
rs1024680 | 0.89[EUR][1000 genomes] |
rs10259565 | 0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10261251 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10267954 | 0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10268288 | 0.91[EUR][1000 genomes] |
rs10269349 | 0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10272641 | 0.88[EUR][1000 genomes] |
rs10275761 | 0.88[EUR][1000 genomes] |
rs10276687 | 0.88[ASN][1000 genomes] |
rs1082028 | 0.87[EUR][1000 genomes] |
rs10951626 | 0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10951627 | 0.80[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs11760739 | 0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11763047 | 0.85[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11767697 | 0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11768838 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11769327 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11980745 | 0.88[EUR][1000 genomes] |
rs12333691 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12333929 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12334141 | 0.84[EUR][1000 genomes] |
rs12530776 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12533272 | 0.87[EUR][1000 genomes] |
rs12534074 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12535524 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1257699 | 0.87[EUR][1000 genomes] |
rs13231777 | 0.84[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13233333 | 0.96[ASN][1000 genomes] |
rs1403381 | 0.88[EUR][1000 genomes] |
rs1406565 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1406566 | 0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1534675 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1568645 | 0.93[EUR][1000 genomes] |
rs1830422 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1874232 | 0.94[ASN][1000 genomes] |
rs1874233 | 0.86[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1881683 | 0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1881684 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1919615 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1973398 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1989589 | 0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2009560 | 0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2019838 | 0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2024200 | 0.87[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2036041 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2052097 | 0.89[EUR][1000 genomes] |
rs2056775 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2109340 | 0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2159488 | 0.88[EUR][1000 genomes] |
rs2329693 | 0.89[EUR][1000 genomes] |
rs2329695 | 0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs28733232 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs33999222 | 0.87[EUR][1000 genomes] |
rs34960564 | 0.92[ASN][1000 genomes] |
rs3847020 | 0.91[EUR][1000 genomes] |
rs3847021 | 0.92[EUR][1000 genomes] |
rs388354 | 0.89[ASN][1000 genomes] |
rs3966459 | 0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4720354 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4723929 | 0.92[EUR][1000 genomes] |
rs4723931 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4723934 | 0.80[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6462961 | 0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6462963 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6462965 | 0.87[ASN][1000 genomes] |
rs66481381 | 0.88[ASN][1000 genomes] |
rs66912039 | 0.86[ASN][1000 genomes] |
rs67438499 | 0.88[ASN][1000 genomes] |
rs6944166 | 0.88[ASN][1000 genomes] |
rs6948982 | 0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6951375 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6952597 | 0.89[EUR][1000 genomes] |
rs6954096 | 0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6957274 | 0.90[ASN][1000 genomes] |
rs6957766 | 0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6960111 | 0.89[EUR][1000 genomes] |
rs6962410 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6963804 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6966917 | 0.88[EUR][1000 genomes] |
rs6968402 | 0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6975853 | 0.92[EUR][1000 genomes] |
rs6978474 | 0.92[ASN][1000 genomes] |
rs6979628 | 0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs71560176 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs731847 | 0.88[EUR][1000 genomes] |
rs731848 | 0.88[EUR][1000 genomes] |
rs773379 | 0.80[EUR][1000 genomes] |
rs773381 | 0.81[EUR][1000 genomes] |
rs773385 | 0.87[EUR][1000 genomes] |
rs773386 | 0.87[EUR][1000 genomes] |
rs773393 | 0.85[EUR][1000 genomes] |
rs773397 | 0.85[EUR][1000 genomes] |
rs773402 | 0.86[EUR][1000 genomes] |
rs773403 | 0.87[EUR][1000 genomes] |
rs773413 | 0.88[EUR][1000 genomes] |
rs773414 | 0.87[EUR][1000 genomes] |
rs773424 | 0.87[EUR][1000 genomes] |
rs7776964 | 0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7776967 | 0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7778061 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7779560 | 0.82[ASN][1000 genomes] |
rs7780858 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7796371 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7797041 | 0.88[EUR][1000 genomes] |
rs7799846 | 0.87[EUR][1000 genomes] |
rs7802584 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7808529 | 0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7809368 | 0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7810509 | 1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs887445 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs887447 | 0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9639818 | 0.89[EUR][1000 genomes] |
rs9639824 | 0.86[ASN][1000 genomes] |
rs9690188 | 0.87[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9791485 | 0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2756801 | chr7:40060180-40269583 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
2 | esv2759525 | chr7:40060180-40269583 | Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
3 | nsv887979 | chr7:40067021-40193535 | Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
4 | nsv887980 | chr7:40067021-40203356 | Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
5 | nsv887981 | chr7:40075461-40203356 | Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
6 | nsv971193 | chr7:40075881-40197955 | Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
7 | esv34547 | chr7:40077032-40230965 | Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
8 | nsv824080 | chr7:40077089-40198644 | Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
9 | nsv464437 | chr7:40094641-40197168 | Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
10 | nsv606709 | chr7:40094641-40197168 | Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
11 | nsv1032278 | chr7:40097371-40396300 | Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
12 | nsv887982 | chr7:40098787-40193535 | Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
13 | nsv1024735 | chr7:40149227-40203356 | Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:40175000-40187600 | Weak transcription | Pancreas | Pancrea |
2 | chr7:40175200-40185800 | Weak transcription | Colonic Mucosa | Colon |
3 | chr7:40175400-40177000 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
4 | chr7:40175400-40177600 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
5 | chr7:40175400-40178000 | Weak transcription | HSMM | muscle |
6 | chr7:40175400-40180800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
7 | chr7:40175400-40181000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
8 | chr7:40175400-40186000 | Weak transcription | Fetal Intestine Small | intestine |
9 | chr7:40175600-40179400 | Weak transcription | Fetal Kidney | kidney |
10 | chr7:40175600-40184800 | Weak transcription | Fetal Intestine Large | intestine |
11 | chr7:40175600-40186800 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
12 | chr7:40175600-40191000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
13 | chr7:40176200-40179800 | Weak transcription | HepG2 | liver |
14 | chr7:40176400-40179000 | Weak transcription | Liver | Liver |