Variant report
Variant | rs4695367 |
---|---|
Chromosome Location | chr4:48284005-48284006 |
allele | A/G |
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 |
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No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10805167 | 0.87[AFR][1000 genomes] |
rs12499164 | 0.87[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs12510551 | 0.83[AMR][1000 genomes] |
rs12640519 | 0.98[AFR][1000 genomes];0.91[AMR][1000 genomes] |
rs12645266 | 0.91[AMR][1000 genomes] |
rs13127675 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1876835 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2055800 | 0.89[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs2352595 | 0.88[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs2464503 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs2704411 | 0.85[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs309886 | 0.93[AFR][1000 genomes];0.91[AMR][1000 genomes] |
rs309888 | 0.83[AFR][1000 genomes] |
rs309889 | 0.84[AFR][1000 genomes];0.91[AMR][1000 genomes] |
rs309893 | 0.81[AFR][1000 genomes];0.91[AMR][1000 genomes] |
rs309894 | 0.91[AMR][1000 genomes] |
rs309895 | 0.91[AMR][1000 genomes] |
rs409176 | 0.81[AFR][1000 genomes];0.91[AMR][1000 genomes] |
rs4095347 | 0.92[AFR][1000 genomes] |
rs419804 | 0.91[AMR][1000 genomes] |
rs4235154 | 0.83[AMR][1000 genomes] |
rs436979 | 0.91[AMR][1000 genomes] |
rs4478160 | 0.83[AMR][1000 genomes] |
rs4695368 | 0.96[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs6447624 | 0.91[AMR][1000 genomes] |
rs6818382 | 0.81[AFR][1000 genomes] |
rs6819233 | 0.91[AMR][1000 genomes] |
rs7661341 | 0.87[AFR][1000 genomes];0.92[AMR][1000 genomes] |
rs937952 | 0.98[AFR][1000 genomes];0.91[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3447039 | chr4:47822266-48285222 | Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 34 gene(s) | inside rSNPs | diseases |
2 | nsv482316 | chr4:48151953-48338746 | Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
3 | esv2763359 | chr4:48189710-48290233 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 20 gene(s) | inside rSNPs | diseases |
4 | nsv1006610 | chr4:48209294-48415387 | Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
5 | nsv537085 | chr4:48209294-48415387 | Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
6 | nsv470032 | chr4:48251915-48312389 | Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:48277400-48287400 | Weak transcription | K562 | blood |
2 | chr4:48279800-48287400 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
3 | chr4:48283400-48284200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |