Variant report
Variant | rs1890854 |
---|---|
Chromosome Location | chr13:69387686-69387687 |
allele | C/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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr13:69385279..69388108-chr13:69393931..69396561,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11616472 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11617638 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1561395 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1659025 | 1.00[ASN][1000 genomes] |
rs17084220 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17571914 | 0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1770329 | 1.00[ASN][1000 genomes] |
rs28652840 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55994724 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56353826 | 1.00[ASN][1000 genomes] |
rs58016055 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59241487 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs600292 | 1.00[ASN][1000 genomes] |
rs61584421 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61949912 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61949913 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs61949950 | 0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61949952 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs620340 | 1.00[ASN][1000 genomes] |
rs630878 | 1.00[ASN][1000 genomes] |
rs632041 | 1.00[ASN][1000 genomes] |
rs661827 | 1.00[ASN][1000 genomes] |
rs669282 | 1.00[ASN][1000 genomes] |
rs685541 | 1.00[ASN][1000 genomes] |
rs7339058 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1049303 | chr13:69238676-69923558 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv1038918 | chr13:69251052-69919763 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | nsv541829 | chr13:69251052-69919763 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
4 | esv2757540 | chr13:69355636-69392579 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv2759945 | chr13:69355636-69392579 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv471145 | chr13:69375632-69388776 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv976245 | chr13:69383145-69387869 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | esv3518742 | chr13:69385694-69393561 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | esv3518753 | chr13:69385694-69393561 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
10 | nsv826691 | chr13:69385796-69392970 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
11 | nsv818974 | chr13:69387686-69391512 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:69387000-69387800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
2 | chr13:69387000-69388200 | Enhancers | Fetal Heart | heart |
3 | chr13:69387200-69387800 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr13:69387400-69387800 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |