Variant report
Variant | rs73485849 |
---|---|
Chromosome Location | chr6:87992068-87992069 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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rs_ID | r2[population] |
---|---|
rs10488045 | 0.94[EUR][1000 genomes] |
rs10498960 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16878570 | 0.88[EUR][1000 genomes] |
rs16878622 | 0.88[EUR][1000 genomes] |
rs16878638 | 0.88[EUR][1000 genomes] |
rs16878712 | 0.94[EUR][1000 genomes] |
rs16878713 | 0.94[EUR][1000 genomes] |
rs16878729 | 0.91[EUR][1000 genomes] |
rs16878734 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs16878736 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs16878809 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs16878856 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16878863 | 0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16878942 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1925693 | 0.94[EUR][1000 genomes] |
rs41273281 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs41273283 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55647962 | 0.85[EUR][1000 genomes] |
rs56193950 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56678817 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56743579 | 0.88[EUR][1000 genomes] |
rs56847789 | 0.85[EUR][1000 genomes] |
rs56999910 | 0.88[EUR][1000 genomes] |
rs57043501 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57116567 | 0.88[EUR][1000 genomes] |
rs57217108 | 0.88[EUR][1000 genomes] |
rs57421283 | 0.94[EUR][1000 genomes] |
rs57607342 | 0.88[EUR][1000 genomes] |
rs57962992 | 0.85[EUR][1000 genomes] |
rs58269367 | 0.94[EUR][1000 genomes] |
rs58327183 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58474842 | 0.94[EUR][1000 genomes] |
rs58731649 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58735749 | 0.94[EUR][1000 genomes] |
rs58751410 | 0.85[EUR][1000 genomes] |
rs59138817 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59150116 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59214037 | 0.94[EUR][1000 genomes] |
rs59495279 | 0.88[EUR][1000 genomes] |
rs59654654 | 0.87[EUR][1000 genomes] |
rs59875769 | 0.94[EUR][1000 genomes] |
rs60074363 | 0.94[EUR][1000 genomes] |
rs60285195 | 0.94[EUR][1000 genomes] |
rs60544317 | 0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs60845773 | 0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60985818 | 0.81[EUR][1000 genomes] |
rs60994855 | 0.85[EUR][1000 genomes] |
rs61047847 | 0.88[EUR][1000 genomes] |
rs61379368 | 0.94[EUR][1000 genomes] |
rs61705669 | 0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73483720 | 0.94[EUR][1000 genomes] |
rs73483728 | 0.94[EUR][1000 genomes] |
rs73483743 | 0.94[EUR][1000 genomes] |
rs73483749 | 0.94[EUR][1000 genomes] |
rs73483752 | 0.94[EUR][1000 genomes] |
rs73483758 | 0.94[EUR][1000 genomes] |
rs73483760 | 0.94[EUR][1000 genomes] |
rs73483765 | 0.94[EUR][1000 genomes] |
rs73483769 | 0.94[EUR][1000 genomes] |
rs73483771 | 0.91[EUR][1000 genomes] |
rs73483774 | 0.94[EUR][1000 genomes] |
rs73483790 | 0.94[EUR][1000 genomes] |
rs73483796 | 0.94[EUR][1000 genomes] |
rs73483799 | 0.94[EUR][1000 genomes] |
rs73485808 | 0.94[EUR][1000 genomes] |
rs73485811 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs73485813 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs73485815 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs73485820 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73485826 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73485828 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73485831 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73485848 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73499800 | 0.88[EUR][1000 genomes] |
rs73499802 | 0.88[EUR][1000 genomes] |
rs73501611 | 0.85[EUR][1000 genomes] |
rs73501620 | 0.88[EUR][1000 genomes] |
rs73501623 | 0.88[EUR][1000 genomes] |
rs73501629 | 0.88[EUR][1000 genomes] |
rs73501632 | 0.88[EUR][1000 genomes] |
rs73501636 | 0.88[EUR][1000 genomes] |
rs73501638 | 0.88[EUR][1000 genomes] |
rs73501641 | 0.88[EUR][1000 genomes] |
rs73501658 | 0.88[EUR][1000 genomes] |
rs73501662 | 0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758067 | chr6:87817883-87992957 | Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | esv2759453 | chr6:87817883-87992957 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | esv2752763 | chr6:87981595-88001064 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:87970600-87994800 | Weak transcription | Fetal Brain Female | brain |
2 | chr6:87991400-87993400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr6:87991800-87992800 | Enhancers | HMEC | breast |
4 | chr6:87991800-87993000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
5 | chr6:87992000-87992400 | Enhancers | NHEK | skin |
6 | chr6:87992000-87993200 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
7 | chr6:87992000-87993600 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |