Variant report
Variant | rs7662861 |
---|---|
Chromosome Location | chr4:21891925-21891926 |
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] |
---|---|
rs10002190 | 1.00[EUR][1000 genomes] |
rs10002260 | 1.00[EUR][1000 genomes] |
rs10004658 | 1.00[EUR][1000 genomes] |
rs10006346 | 1.00[EUR][1000 genomes] |
rs10028615 | 1.00[EUR][1000 genomes] |
rs10029020 | 1.00[EUR][1000 genomes] |
rs10034459 | 1.00[EUR][1000 genomes] |
rs1034501 | 1.00[EUR][1000 genomes] |
rs1034502 | 1.00[EUR][1000 genomes] |
rs1040038 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1158455 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13102999 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13117670 | 1.00[EUR][1000 genomes] |
rs1398831 | 1.00[EUR][1000 genomes] |
rs1503980 | 1.00[EUR][1000 genomes] |
rs1503981 | 1.00[EUR][1000 genomes] |
rs1543101 | 1.00[EUR][1000 genomes] |
rs1588709 | 1.00[EUR][1000 genomes] |
rs16871729 | 1.00[EUR][1000 genomes] |
rs16871771 | 1.00[EUR][1000 genomes] |
rs16871794 | 1.00[EUR][1000 genomes] |
rs16871797 | 1.00[EUR][1000 genomes] |
rs16871821 | 1.00[EUR][1000 genomes] |
rs16871823 | 1.00[EUR][1000 genomes] |
rs16871835 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16871838 | 1.00[EUR][1000 genomes] |
rs16871877 | 1.00[EUR][1000 genomes] |
rs16871884 | 1.00[EUR][1000 genomes] |
rs187237 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1877612 | 1.00[EUR][1000 genomes] |
rs2044806 | 1.00[EUR][1000 genomes] |
rs2137651 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28377254 | 1.00[EUR][1000 genomes] |
rs28378411 | 1.00[EUR][1000 genomes] |
rs28379124 | 1.00[EUR][1000 genomes] |
rs28399840 | 1.00[EUR][1000 genomes] |
rs28456170 | 1.00[EUR][1000 genomes] |
rs28463803 | 1.00[EUR][1000 genomes] |
rs28560247 | 1.00[EUR][1000 genomes] |
rs28578090 | 1.00[EUR][1000 genomes] |
rs28662772 | 1.00[EUR][1000 genomes] |
rs360689 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs360699 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4101628 | 1.00[EUR][1000 genomes] |
rs4235292 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4289435 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4438750 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4696983 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4696987 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs4696990 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4697239 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4697240 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4697242 | 1.00[EUR][1000 genomes] |
rs4697245 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55820441 | 1.00[EUR][1000 genomes] |
rs55906210 | 1.00[EUR][1000 genomes] |
rs57298063 | 1.00[EUR][1000 genomes] |
rs58744364 | 1.00[EUR][1000 genomes] |
rs59037882 | 1.00[EUR][1000 genomes] |
rs59247815 | 1.00[EUR][1000 genomes] |
rs6448090 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6810989 | 1.00[EUR][1000 genomes] |
rs6814288 | 1.00[EUR][1000 genomes] |
rs6819373 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6821199 | 1.00[EUR][1000 genomes] |
rs6835916 | 1.00[EUR][1000 genomes] |
rs6836067 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6836263 | 1.00[EUR][1000 genomes] |
rs6836739 | 1.00[EUR][1000 genomes] |
rs6840933 | 1.00[EUR][1000 genomes] |
rs7438259 | 1.00[EUR][1000 genomes] |
rs7442181 | 1.00[AMR][1000 genomes] |
rs7656388 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7666663 | 1.00[EUR][1000 genomes] |
rs7671356 | 1.00[EUR][1000 genomes] |
rs7671527 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7672938 | 1.00[EUR][1000 genomes] |
rs7683672 | 1.00[EUR][1000 genomes] |
rs7688144 | 1.00[EUR][1000 genomes] |
rs7689554 | 1.00[EUR][1000 genomes] |
rs907788 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs907789 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs971878 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9784415 | 1.00[EUR][1000 genomes] |
rs9991631 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9996615 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817467 | chr4:21602921-22422816 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | esv2757924 | chr4:21873204-21980559 | Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv2759231 | chr4:21873204-21980559 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv428440 | chr4:21873204-21980559 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:21890400-21893200 | Weak transcription | Ovary | ovary |
2 | chr4:21890600-21894600 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
3 | chr4:21890600-21894800 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
4 | chr4:21891000-21892400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr4:21891200-21899600 | Weak transcription | HMEC | breast |
6 | chr4:21891400-21894600 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
7 | chr4:21891600-21894400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |