Variant report
Variant | rs9829189 |
---|---|
Chromosome Location | chr3:158950225-158950226 |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:158949275..158950779-chr3:158953655..158955845,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10470473 | 0.85[EUR][1000 genomes] |
rs10513537 | 0.85[EUR][1000 genomes] |
rs10936173 | 0.84[EUR][1000 genomes] |
rs11924990 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1449021 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17727250 | 0.85[EUR][1000 genomes] |
rs1868414 | 0.82[ASN][1000 genomes] |
rs2122147 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs2365483 | 0.84[EUR][1000 genomes] |
rs2365490 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs4679855 | 0.84[EUR][1000 genomes] |
rs4680497 | 0.84[EUR][1000 genomes] |
rs4680498 | 0.84[EUR][1000 genomes] |
rs58290749 | 0.84[EUR][1000 genomes] |
rs6441253 | 0.87[AMR][1000 genomes] |
rs6781221 | 0.87[AMR][1000 genomes] |
rs720397 | 0.83[ASN][1000 genomes] |
rs9820047 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9823142 | 1.00[ASN][1000 genomes] |
rs9827242 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9827400 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs9831067 | 0.87[AMR][1000 genomes] |
rs9834328 | 1.00[ASN][1000 genomes] |
rs9839112 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs9840972 | 0.85[EUR][1000 genomes] |
rs9852196 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9856166 | 0.84[EUR][1000 genomes] |
rs9862769 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9878883 | 0.85[EUR][1000 genomes] |
rs9880642 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530059 | chr3:158332590-159147549 | Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
2 | nsv470971 | chr3:158590928-159158217 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
3 | esv3426016 | chr3:158676623-158979242 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv491927 | chr3:158692653-158952780 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv998949 | chr3:158774806-159394550 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1012602 | chr3:158800182-159031618 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv966965 | chr3:158947307-158950936 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:158949200-158952000 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |