Variant report
| Variant | rs17105375 |
|---|---|
| Chromosome Location | chr14:37269137-37269138 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:2 , 50 per page) page:
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rSNPs within LD-proxies of this variant (count:18)
| rs_ID | r2[population] |
|---|---|
| rs1429846 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17105258 | 0.82[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17105317 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17105336 | 1.00[YRI][hapmap] |
| rs17105389 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17105392 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17105396 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17105423 | 1.00[EUR][1000 genomes] |
| rs17105467 | 1.00[EUR][1000 genomes] |
| rs1950353 | 1.00[EUR][1000 genomes] |
| rs2415362 | 1.00[EUR][1000 genomes] |
| rs28633981 | 1.00[AMR][1000 genomes] |
| rs55733140 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6571763 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs74044987 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs74045000 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs74045208 | 1.00[AMR][1000 genomes] |
| rs8007647 | 1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1047290 | chr14:36564568-37445157 | Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 43 gene(s) | inside rSNPs | diseases |
| 2 | nsv1037952 | chr14:36670484-37294692 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
| 3 | nsv542042 | chr14:36670484-37294692 | Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
| 4 | nsv534288 | chr14:37254539-37697745 | Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 17 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
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