Variant report
Variant | rs286626 |
---|---|
Chromosome Location | chr5:154416563-154416564 |
allele | C/T |
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] |
---|---|
rs10057198 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs101271 | 0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1603404 | 0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs166989 | 0.89[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2431154 | 0.81[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs2431156 | 0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2453756 | 0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs286620 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs286630 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs286631 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs287117 | 0.93[AFR][1000 genomes] |
rs287118 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs287121 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs287123 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs287124 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28775325 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs412109 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs445362 | 0.93[AFR][1000 genomes] |
rs664586 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7443026 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv883058 | chr5:154375465-154432580 | Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | esv3374550 | chr5:154403808-154421409 | Enhancers Weak transcription Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
3 | esv3410951 | chr5:154403808-154427370 | Enhancers Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
4 | nsv1023588 | chr5:154415586-154464455 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:154416000-154416800 | Active TSS | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |