Variant report
Variant | rs67403526 |
---|---|
Chromosome Location | chr3:160341103-160341104 |
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] |
---|---|
rs2305401 | 0.95[ASN][1000 genomes] |
rs3736627 | 0.80[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3806629 | 0.84[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs56124988 | 0.95[ASN][1000 genomes] |
rs56333234 | 0.85[EUR][1000 genomes] |
rs56343019 | 0.95[ASN][1000 genomes] |
rs56396435 | 0.85[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs57050097 | 0.90[ASN][1000 genomes] |
rs57277659 | 0.82[ASN][1000 genomes] |
rs57328745 | 0.85[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs57555307 | 0.95[ASN][1000 genomes] |
rs58377812 | 0.86[ASN][1000 genomes] |
rs59364034 | 0.85[EUR][1000 genomes] |
rs59695030 | 0.80[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs60066272 | 0.95[ASN][1000 genomes] |
rs60517889 | 0.90[ASN][1000 genomes] |
rs62272209 | 0.85[EUR][1000 genomes] |
rs62272210 | 0.85[EUR][1000 genomes] |
rs62272213 | 0.85[EUR][1000 genomes] |
rs62272221 | 0.81[EUR][1000 genomes] |
rs62272229 | 0.81[EUR][1000 genomes] |
rs62272249 | 0.82[ASN][1000 genomes] |
rs62272251 | 0.82[ASN][1000 genomes] |
rs62272254 | 0.90[ASN][1000 genomes] |
rs62272255 | 0.90[ASN][1000 genomes] |
rs62272256 | 0.90[ASN][1000 genomes] |
rs62272257 | 0.90[ASN][1000 genomes] |
rs62272258 | 0.90[ASN][1000 genomes] |
rs62272259 | 0.90[ASN][1000 genomes] |
rs62272780 | 0.95[ASN][1000 genomes] |
rs62272781 | 0.95[ASN][1000 genomes] |
rs62272783 | 0.95[ASN][1000 genomes] |
rs62272785 | 0.95[ASN][1000 genomes] |
rs62272787 | 0.95[ASN][1000 genomes] |
rs62272788 | 0.95[ASN][1000 genomes] |
rs62272790 | 0.80[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62272793 | 0.80[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62272799 | 0.84[ASN][1000 genomes] |
rs62272804 | 0.95[ASN][1000 genomes] |
rs62272805 | 0.95[ASN][1000 genomes] |
rs62272806 | 0.84[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62272831 | 0.84[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62272833 | 0.85[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62272836 | 0.85[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62272838 | 0.85[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs73155914 | 0.95[ASN][1000 genomes] |
rs73155963 | 0.85[EUR][1000 genomes] |
rs7648832 | 0.90[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532666 | chr3:159777847-160703202 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 271 gene(s) | inside rSNPs | diseases |
2 | nsv1000453 | chr3:159853305-160366357 | Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 259 gene(s) | inside rSNPs | diseases |
3 | nsv536779 | chr3:159853305-160366357 | Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 259 gene(s) | inside rSNPs | diseases |
4 | nsv877703 | chr3:160325458-160398885 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:160338600-160342400 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
2 | chr3:160339400-160341200 | Enhancers | Liver | Liver |
3 | chr3:160339600-160341200 | Enhancers | Muscle Satellite Cultured Cells | -- |