Variant report
Variant | rs34880892 |
---|---|
Chromosome Location | chr5:43362545-43362546 |
allele | A/C |
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] |
---|---|
rs10043868 | 0.97[ASN][1000 genomes] |
rs10044795 | 0.91[ASN][1000 genomes] |
rs10044799 | 0.97[ASN][1000 genomes] |
rs10062256 | 0.97[ASN][1000 genomes] |
rs1025299 | 0.97[ASN][1000 genomes] |
rs10473309 | 0.94[ASN][1000 genomes] |
rs1083833 | 0.91[ASN][1000 genomes] |
rs10941618 | 1.00[AMR][1000 genomes] |
rs12656248 | 1.00[EUR][1000 genomes] |
rs13154319 | 1.00[AMR][1000 genomes] |
rs13155023 | 1.00[AMR][1000 genomes] |
rs13155622 | 1.00[AMR][1000 genomes] |
rs13159247 | 1.00[EUR][1000 genomes] |
rs13160431 | 1.00[EUR][1000 genomes] |
rs13164705 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs13165339 | 1.00[AMR][1000 genomes] |
rs13167052 | 1.00[AMR][1000 genomes] |
rs13167785 | 1.00[EUR][1000 genomes] |
rs13167974 | 1.00[EUR][1000 genomes] |
rs13168456 | 1.00[AMR][1000 genomes] |
rs13169908 | 1.00[AMR][1000 genomes] |
rs13174298 | 1.00[AMR][1000 genomes] |
rs13186439 | 1.00[AMR][1000 genomes] |
rs13190188 | 1.00[EUR][1000 genomes] |
rs28461402 | 0.97[ASN][1000 genomes] |
rs34057521 | 1.00[EUR][1000 genomes] |
rs34060183 | 0.97[ASN][1000 genomes] |
rs34087297 | 1.00[EUR][1000 genomes] |
rs34150414 | 1.00[AMR][1000 genomes] |
rs34181466 | 1.00[EUR][1000 genomes] |
rs34238140 | 1.00[AMR][1000 genomes] |
rs34353246 | 1.00[EUR][1000 genomes] |
rs34379498 | 1.00[AMR][1000 genomes] |
rs34497448 | 1.00[AMR][1000 genomes] |
rs34709217 | 1.00[AMR][1000 genomes] |
rs34762186 | 1.00[AMR][1000 genomes] |
rs34965256 | 1.00[AMR][1000 genomes] |
rs35001439 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35033162 | 1.00[AMR][1000 genomes] |
rs35141306 | 1.00[EUR][1000 genomes] |
rs35142013 | 1.00[AMR][1000 genomes] |
rs35350677 | 1.00[AMR][1000 genomes] |
rs35446538 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35748848 | 1.00[AMR][1000 genomes] |
rs35756093 | 1.00[AMR][1000 genomes] |
rs36000604 | 1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs36025143 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs36036217 | 1.00[AMR][1000 genomes] |
rs36062172 | 1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs36063200 | 0.97[ASN][1000 genomes] |
rs36097388 | 1.00[AMR][1000 genomes] |
rs3733767 | 0.97[ASN][1000 genomes] |
rs3756417 | 0.81[ASN][1000 genomes] |
rs3797152 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs3797153 | 0.97[ASN][1000 genomes] |
rs3806871 | 1.00[AMR][1000 genomes] |
rs3822423 | 0.97[ASN][1000 genomes] |
rs6451687 | 0.97[ASN][1000 genomes] |
rs6451688 | 0.97[ASN][1000 genomes] |
rs6861429 | 0.97[ASN][1000 genomes] |
rs6862588 | 0.97[ASN][1000 genomes] |
rs6865915 | 0.94[ASN][1000 genomes] |
rs6866007 | 0.91[ASN][1000 genomes] |
rs6868939 | 0.80[ASN][1000 genomes] |
rs6878207 | 0.89[ASN][1000 genomes] |
rs6892337 | 0.97[ASN][1000 genomes] |
rs71590642 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs71610306 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs71627597 | 1.00[AMR][1000 genomes] |
rs71627598 | 1.00[AMR][1000 genomes] |
rs71627599 | 1.00[AMR][1000 genomes] |
rs71627600 | 1.00[AMR][1000 genomes] |
rs71629106 | 1.00[AMR][1000 genomes] |
rs71629107 | 0.97[ASN][1000 genomes] |
rs71629168 | 1.00[EUR][1000 genomes] |
rs71629169 | 1.00[EUR][1000 genomes] |
rs9292877 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv508352 | chr5:43237830-43391062 | Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:43362200-43364000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |