Variant report
Variant | rs1512303 |
---|---|
Chromosome Location | chr4:45155708-45155709 |
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] |
---|---|
rs10024284 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10024389 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10084781 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10084782 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10084842 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10084859 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10213047 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10470763 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10938386 | 1.00[ASN][1000 genomes] |
rs1159117 | 1.00[ASN][1000 genomes] |
rs1159118 | 1.00[ASN][1000 genomes] |
rs11729006 | 1.00[ASN][1000 genomes] |
rs11941164 | 1.00[ASN][1000 genomes] |
rs12640145 | 1.00[ASN][1000 genomes] |
rs13106713 | 1.00[ASN][1000 genomes] |
rs13133961 | 1.00[ASN][1000 genomes] |
rs13142361 | 1.00[ASN][1000 genomes] |
rs13146241 | 1.00[ASN][1000 genomes] |
rs1319519 | 0.88[ASN][1000 genomes] |
rs13434591 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13434955 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1512300 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1512305 | 1.00[ASN][1000 genomes] |
rs1512313 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1512314 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1512316 | 1.00[ASN][1000 genomes] |
rs1512317 | 1.00[ASN][1000 genomes] |
rs1512318 | 1.00[ASN][1000 genomes] |
rs1512319 | 1.00[ASN][1000 genomes] |
rs1512320 | 1.00[ASN][1000 genomes] |
rs1512321 | 1.00[ASN][1000 genomes] |
rs1606314 | 1.00[ASN][1000 genomes] |
rs1606315 | 1.00[ASN][1000 genomes] |
rs1606316 | 1.00[ASN][1000 genomes] |
rs1606317 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1606318 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17470619 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17470661 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17574252 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17574419 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17574467 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1849329 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1849333 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1849334 | 1.00[ASN][1000 genomes] |
rs1849337 | 1.00[ASN][1000 genomes] |
rs1858413 | 1.00[ASN][1000 genomes] |
rs1858414 | 1.00[ASN][1000 genomes] |
rs1960115 | 1.00[ASN][1000 genomes] |
rs2048542 | 1.00[ASN][1000 genomes] |
rs2048543 | 1.00[ASN][1000 genomes] |
rs2048544 | 1.00[ASN][1000 genomes] |
rs2048545 | 1.00[ASN][1000 genomes] |
rs2102595 | 1.00[ASN][1000 genomes] |
rs2348812 | 1.00[ASN][1000 genomes] |
rs28547392 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28595673 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28787380 | 0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs28819701 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2882028 | 1.00[ASN][1000 genomes] |
rs28871337 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4305555 | 1.00[ASN][1000 genomes] |
rs4306991 | 1.00[ASN][1000 genomes] |
rs4317235 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4321671 | 1.00[ASN][1000 genomes] |
rs4371653 | 1.00[ASN][1000 genomes] |
rs4376184 | 1.00[ASN][1000 genomes] |
rs4404583 | 1.00[ASN][1000 genomes] |
rs4422445 | 1.00[ASN][1000 genomes] |
rs4432781 | 1.00[ASN][1000 genomes] |
rs4444869 | 1.00[ASN][1000 genomes] |
rs4473684 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4481272 | 1.00[ASN][1000 genomes] |
rs4492039 | 1.00[ASN][1000 genomes] |
rs4493580 | 0.96[ASN][1000 genomes] |
rs4586989 | 1.00[ASN][1000 genomes] |
rs4586990 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4604088 | 1.00[ASN][1000 genomes] |
rs4624697 | 1.00[ASN][1000 genomes] |
rs4642285 | 1.00[ASN][1000 genomes] |
rs4642286 | 1.00[ASN][1000 genomes] |
rs4643858 | 1.00[ASN][1000 genomes] |
rs4974508 | 1.00[ASN][1000 genomes] |
rs4974513 | 1.00[ASN][1000 genomes] |
rs62409604 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409606 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409607 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409613 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409614 | 0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62409615 | 0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62409621 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs62409624 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs62409625 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409626 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409627 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409628 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409629 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409630 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409632 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409634 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409639 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409642 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62409643 | 0.96[EUR][1000 genomes] |
rs62409870 | 1.00[ASN][1000 genomes] |
rs62409874 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62411632 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62411633 | 1.00[ASN][1000 genomes] |
rs62411634 | 1.00[ASN][1000 genomes] |
rs62411635 | 1.00[ASN][1000 genomes] |
rs62411637 | 1.00[ASN][1000 genomes] |
rs62411638 | 1.00[ASN][1000 genomes] |
rs62411640 | 1.00[ASN][1000 genomes] |
rs62411641 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62411642 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6414673 | 1.00[ASN][1000 genomes] |
rs6447414 | 1.00[ASN][1000 genomes] |
rs6447417 | 1.00[ASN][1000 genomes] |
rs6447425 | 1.00[ASN][1000 genomes] |
rs6447426 | 1.00[ASN][1000 genomes] |
rs6447429 | 1.00[ASN][1000 genomes] |
rs6447436 | 1.00[ASN][1000 genomes] |
rs6814348 | 1.00[ASN][1000 genomes] |
rs6815872 | 1.00[ASN][1000 genomes] |
rs6817044 | 1.00[ASN][1000 genomes] |
rs6855504 | 1.00[ASN][1000 genomes] |
rs6856726 | 1.00[ASN][1000 genomes] |
rs7654727 | 1.00[ASN][1000 genomes] |
rs7656136 | 1.00[ASN][1000 genomes] |
rs7659477 | 1.00[ASN][1000 genomes] |
rs7663667 | 1.00[ASN][1000 genomes] |
rs7669613 | 1.00[ASN][1000 genomes] |
rs7669811 | 1.00[ASN][1000 genomes] |
rs7677867 | 1.00[ASN][1000 genomes] |
rs7690331 | 1.00[ASN][1000 genomes] |
rs9917913 | 1.00[ASN][1000 genomes] |
rs991982 | 1.00[ASN][1000 genomes] |
rs996002 | 1.00[ASN][1000 genomes] |
rs996003 | 1.00[ASN][1000 genomes] |
rs9992572 | 1.00[ASN][1000 genomes] |
rs9999206 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531944 | chr4:44299343-45200700 | Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
2 | nsv1014327 | chr4:44735209-45218149 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv829919 | chr4:45069901-45253808 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv594104 | chr4:45105210-45665828 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:45125800-45174400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr4:45150400-45157200 | Weak transcription | HSMM | muscle |
3 | chr4:45150600-45156800 | Weak transcription | Muscle Satellite Cultured Cells | -- |