Variant report
Variant | rs6814143 |
---|---|
Chromosome Location | chr4:76136757-76136758 |
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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10000494 | 0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10006152 | 0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10006801 | 0.96[ASN][1000 genomes] |
rs10021538 | 0.80[ASN][1000 genomes] |
rs10033452 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11722701 | 0.92[ASN][1000 genomes] |
rs11725912 | 0.92[ASN][1000 genomes] |
rs12643174 | 0.85[AFR][1000 genomes] |
rs13102259 | 0.92[ASN][1000 genomes] |
rs13102557 | 0.83[ASN][1000 genomes] |
rs1497205 | 0.92[ASN][1000 genomes] |
rs1497206 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1497207 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1497226 | 0.93[ASN][1000 genomes] |
rs1506592 | 0.96[ASN][1000 genomes] |
rs1506593 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1874585 | 0.92[ASN][1000 genomes] |
rs2132800 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs2132804 | 0.92[ASN][1000 genomes] |
rs2132806 | 0.93[ASN][1000 genomes] |
rs28505529 | 0.85[AFR][1000 genomes] |
rs28654917 | 0.85[AFR][1000 genomes] |
rs28682501 | 0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs55950539 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6535241 | 0.93[ASN][1000 genomes] |
rs6811197 | 0.82[ASN][1000 genomes] |
rs6848890 | 0.96[ASN][1000 genomes] |
rs6850048 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6851300 | 0.96[ASN][1000 genomes] |
rs6854668 | 0.87[ASN][1000 genomes] |
rs6857874 | 0.88[ASN][1000 genomes] |
rs6858597 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7656435 | 0.96[ASN][1000 genomes] |
rs7658434 | 0.92[ASN][1000 genomes] |
rs7670647 | 0.95[ASN][1000 genomes] |
rs7673324 | 0.92[ASN][1000 genomes] |
rs7676316 | 0.90[ASN][1000 genomes] |
rs7677215 | 0.96[ASN][1000 genomes] |
rs7681167 | 0.96[ASN][1000 genomes] |
rs7685095 | 0.82[ASN][1000 genomes] |
rs7689597 | 0.95[ASN][1000 genomes] |
rs7691721 | 0.92[ASN][1000 genomes] |
rs9307717 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1005324 | chr4:75689880-76233555 | Bivalent/Poised TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv537142 | chr4:75689880-76233555 | Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
3 | nsv1010552 | chr4:76064415-76325430 | Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
4 | esv1850883 | chr4:76065572-76194403 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv879492 | chr4:76088845-76154064 | Enhancers Active TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:76135400-76138200 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
2 | chr4:76135600-76137000 | Enhancers | Fetal Muscle Leg | muscle |