Variant report
Variant | rs9967444 |
---|---|
Chromosome Location | chr18:39886320-39886321 |
allele | C/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] |
---|---|
rs10502781 | 0.87[EUR][1000 genomes] |
rs10502782 | 0.97[ASN][1000 genomes] |
rs10502783 | 1.00[ASN][1000 genomes] |
rs11082269 | 1.00[ASN][1000 genomes] |
rs11874061 | 1.00[ASN][1000 genomes] |
rs12604128 | 1.00[ASN][1000 genomes] |
rs12967992 | 0.86[ASN][1000 genomes] |
rs1381344 | 0.84[ASN][1000 genomes] |
rs1381345 | 1.00[ASN][1000 genomes] |
rs1461704 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs17610303 | 0.89[EUR][1000 genomes] |
rs4890232 | 0.81[ASN][1000 genomes] |
rs56145428 | 0.86[EUR][1000 genomes] |
rs7228908 | 0.87[EUR][1000 genomes] |
rs7230352 | 0.86[EUR][1000 genomes] |
rs7235200 | 1.00[ASN][1000 genomes] |
rs7240321 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72901342 | 0.85[EUR][1000 genomes] |
rs72901344 | 0.89[EUR][1000 genomes] |
rs72901345 | 0.86[EUR][1000 genomes] |
rs72901351 | 0.85[EUR][1000 genomes] |
rs72901355 | 0.87[EUR][1000 genomes] |
rs72901367 | 0.89[EUR][1000 genomes] |
rs72901374 | 0.86[EUR][1000 genomes] |
rs72901375 | 0.85[EUR][1000 genomes] |
rs72901378 | 0.86[EUR][1000 genomes] |
rs8089535 | 1.00[ASN][1000 genomes] |
rs9946713 | 0.85[ASN][1000 genomes] |
rs9955570 | 0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949609 | chr18:39126941-40070286 | Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 11 gene(s) | inside rSNPs | diseases |
2 | nsv1059409 | chr18:39711099-40139446 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1063343 | chr18:39760943-39898498 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:39883600-39887800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr18:39885800-39886400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |