Variant report
Variant | rs9852974 |
---|---|
Chromosome Location | chr3:158099462-158099463 |
allele | C/T |
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 | chr3:158093335..158095765-chr3:158098415..158100643,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10049160 | 1.00[EUR][1000 genomes] |
rs12330339 | 1.00[EUR][1000 genomes] |
rs13321065 | 0.97[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs13322986 | 1.00[EUR][1000 genomes] |
rs13323462 | 1.00[EUR][1000 genomes] |
rs16829007 | 0.80[YRI][hapmap];1.00[EUR][1000 genomes] |
rs28396261 | 1.00[EUR][1000 genomes] |
rs28402668 | 1.00[EUR][1000 genomes] |
rs28428827 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28506940 | 1.00[EUR][1000 genomes] |
rs28608522 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28646251 | 1.00[EUR][1000 genomes] |
rs28680366 | 1.00[EUR][1000 genomes] |
rs28720767 | 1.00[EUR][1000 genomes] |
rs56987573 | 0.94[AFR][1000 genomes] |
rs6441190 | 1.00[EUR][1000 genomes] |
rs6441192 | 1.00[EUR][1000 genomes] |
rs6762087 | 1.00[EUR][1000 genomes] |
rs6762923 | 1.00[EUR][1000 genomes] |
rs6765159 | 1.00[EUR][1000 genomes] |
rs6767072 | 1.00[EUR][1000 genomes] |
rs6775960 | 1.00[EUR][1000 genomes] |
rs6776674 | 1.00[EUR][1000 genomes] |
rs6784612 | 0.97[YRI][hapmap];0.91[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6784707 | 0.96[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6786770 | 1.00[EUR][1000 genomes] |
rs6787212 | 1.00[EUR][1000 genomes] |
rs6789607 | 1.00[EUR][1000 genomes] |
rs6798405 | 0.90[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6801076 | 1.00[EUR][1000 genomes] |
rs6804113 | 1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6806720 | 0.85[AFR][1000 genomes] |
rs6809280 | 1.00[EUR][1000 genomes] |
rs6810324 | 1.00[EUR][1000 genomes] |
rs73013336 | 0.92[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73017472 | 1.00[EUR][1000 genomes] |
rs73027918 | 1.00[EUR][1000 genomes] |
rs73028000 | 1.00[EUR][1000 genomes] |
rs73028775 | 1.00[EUR][1000 genomes] |
rs73028779 | 1.00[EUR][1000 genomes] |
rs73029897 | 1.00[EUR][1000 genomes] |
rs73029899 | 1.00[EUR][1000 genomes] |
rs73030514 | 1.00[EUR][1000 genomes] |
rs73031618 | 1.00[EUR][1000 genomes] |
rs73031643 | 1.00[EUR][1000 genomes] |
rs73031646 | 1.00[EUR][1000 genomes] |
rs7613737 | 1.00[EUR][1000 genomes] |
rs7615598 | 0.97[YRI][hapmap] |
rs7618252 | 1.00[EUR][1000 genomes] |
rs7621282 | 1.00[EUR][1000 genomes] |
rs7622013 | 1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7627082 | 1.00[EUR][1000 genomes] |
rs7633366 | 1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7635356 | 1.00[EUR][1000 genomes] |
rs7638647 | 1.00[EUR][1000 genomes] |
rs9817119 | 1.00[EUR][1000 genomes] |
rs9821945 | 1.00[EUR][1000 genomes] |
rs9824822 | 0.97[YRI][hapmap];0.93[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs9829790 | 0.83[YRI][hapmap];1.00[EUR][1000 genomes] |
rs9838425 | 1.00[EUR][1000 genomes] |
rs9841653 | 1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9843252 | 1.00[EUR][1000 genomes] |
rs9846272 | 1.00[EUR][1000 genomes] |
rs9852177 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9861869 | 1.00[EUR][1000 genomes] |
rs9863618 | 1.00[EUR][1000 genomes] |
rs9868975 | 1.00[EUR][1000 genomes] |
rs9869501 | 1.00[EUR][1000 genomes] |
rs9870885 | 1.00[EUR][1000 genomes] |
rs9872642 | 1.00[EUR][1000 genomes] |
rs9873074 | 1.00[EUR][1000 genomes] |
rs9877427 | 1.00[EUR][1000 genomes] |
rs9877843 | 1.00[EUR][1000 genomes] |
rs9877873 | 1.00[EUR][1000 genomes] |
rs9878828 | 1.00[EUR][1000 genomes] |
rs9882507 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1013391 | chr3:157505943-158115553 | Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv536775 | chr3:157505943-158115553 | Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv1002378 | chr3:157715428-158673414 | Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
4 | nsv877689 | chr3:157858930-158133307 | Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv916910 | chr3:157926799-158183372 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1014381 | chr3:158070451-158350118 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
7 | nsv1000904 | chr3:158094357-158159317 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:158098800-158099600 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |