Variant report
Variant | rs73025882 |
---|---|
Chromosome Location | chr3:156608036-156608037 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:156603770..156606924-chr3:156607944..156610272,5 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11918032 | 1.00[EUR][1000 genomes] |
rs11918873 | 1.00[EUR][1000 genomes] |
rs11918949 | 1.00[EUR][1000 genomes] |
rs11921057 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11925276 | 1.00[EUR][1000 genomes] |
rs1482867 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16827186 | 1.00[AMR][1000 genomes] |
rs16827190 | 1.00[EUR][1000 genomes] |
rs16827209 | 1.00[EUR][1000 genomes] |
rs56772168 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56984599 | 1.00[EUR][1000 genomes] |
rs57454874 | 1.00[EUR][1000 genomes] |
rs57676345 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58897582 | 1.00[EUR][1000 genomes] |
rs59516322 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61469347 | 1.00[EUR][1000 genomes] |
rs6441110 | 1.00[EUR][1000 genomes] |
rs6774975 | 1.00[EUR][1000 genomes] |
rs6778746 | 1.00[EUR][1000 genomes] |
rs6788106 | 1.00[EUR][1000 genomes] |
rs6789293 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6791852 | 1.00[EUR][1000 genomes] |
rs6793139 | 1.00[EUR][1000 genomes] |
rs73013921 | 1.00[EUR][1000 genomes] |
rs73013929 | 1.00[EUR][1000 genomes] |
rs73013931 | 1.00[EUR][1000 genomes] |
rs73013985 | 1.00[EUR][1000 genomes] |
rs73014000 | 1.00[EUR][1000 genomes] |
rs73015891 | 1.00[EUR][1000 genomes] |
rs73017741 | 1.00[EUR][1000 genomes] |
rs73019707 | 1.00[EUR][1000 genomes] |
rs73019709 | 1.00[EUR][1000 genomes] |
rs73019730 | 1.00[EUR][1000 genomes] |
rs73019732 | 1.00[EUR][1000 genomes] |
rs73019733 | 1.00[EUR][1000 genomes] |
rs73021795 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73021801 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73025844 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73025863 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73025895 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73025901 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73027741 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73027753 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73027764 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73029518 | 1.00[EUR][1000 genomes] |
rs73029521 | 1.00[EUR][1000 genomes] |
rs73029526 | 1.00[EUR][1000 genomes] |
rs7612186 | 1.00[EUR][1000 genomes] |
rs7621847 | 1.00[EUR][1000 genomes] |
rs7623810 | 1.00[EUR][1000 genomes] |
rs7634624 | 1.00[EUR][1000 genomes] |
rs7635251 | 1.00[AMR][1000 genomes] |
rs7645166 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7652081 | 0.84[AFR][1000 genomes];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 | nsv877685 | chr3:156444383-156611676 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 48 gene(s) | inside rSNPs | diseases |
2 | nsv829765 | chr3:156568263-156718496 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:156598200-156609600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr3:156607400-156610000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
3 | chr3:156607600-156610600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
4 | chr3:156607800-156609600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |