Variant report
| Variant | rs4252108 |
|---|---|
| Chromosome Location | chr6:161137523-161137524 |
| allele | A/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 | chr6:161135262..161137526-chr6:161141388..161143611,2 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:23)
| rs_ID | r2[population] |
|---|---|
| rs1130656 | 1.00[ASN][1000 genomes] |
| rs1321201 | 0.97[ASN][1000 genomes] |
| rs14224 | 1.00[ASN][1000 genomes] |
| rs1465620 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
| rs1594307 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs1652508 | 0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes] |
| rs1830519 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
| rs2295368 | 1.00[ASN][1000 genomes] |
| rs2859879 | 0.81[AMR][1000 genomes] |
| rs3757017 | 0.81[AMR][1000 genomes] |
| rs3757019 | 0.94[ASN][1000 genomes] |
| rs3778217 | 0.90[ASN][1000 genomes] |
| rs3798903 | 0.96[ASN][1000 genomes] |
| rs3823055 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs4252075 | 0.94[ASN][1000 genomes] |
| rs4252092 | 0.96[ASN][1000 genomes] |
| rs4252105 | 0.97[ASN][1000 genomes] |
| rs4709458 | 0.81[ASN][1000 genomes] |
| rs4709460 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
| rs4709461 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs783146 | 0.92[ASN][1000 genomes] |
| rs783147 | 0.92[ASN][1000 genomes] |
| rs9295131 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | esv2758089 | chr6:160372244-161234665 | Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
| 2 | esv2759484 | chr6:160372244-161234665 | Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
| 3 | nsv605005 | chr6:161069941-161152449 | Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
| 4 | nsv1019113 | chr6:161127584-161197558 | Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:161131200-161138800 | Genic enhancers | Liver | Liver |
| 2 | chr6:161137000-161137600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
