Variant report
Variant | rs11265443 |
---|---|
Chromosome Location | chr1:160564683-160564684 |
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] |
---|---|
rs1061217 | 0.81[ASN][1000 genomes] |
rs10752638 | 0.81[ASN][1000 genomes] |
rs10797083 | 0.82[ASN][1000 genomes] |
rs10908789 | 0.85[ASN][1000 genomes] |
rs10908792 | 0.92[ASN][1000 genomes] |
rs10908794 | 0.82[ASN][1000 genomes] |
rs10908796 | 0.81[ASN][1000 genomes] |
rs11265442 | 0.86[ASN][1000 genomes] |
rs11265444 | 0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11265449 | 0.81[EUR][1000 genomes] |
rs12402879 | 0.83[ASN][1000 genomes] |
rs12736781 | 0.85[ASN][1000 genomes] |
rs1394079 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1572382 | 0.82[ASN][1000 genomes] |
rs1604783 | 0.82[ASN][1000 genomes] |
rs6427535 | 0.81[ASN][1000 genomes] |
rs6668760 | 0.83[ASN][1000 genomes] |
rs6692382 | 0.83[ASN][1000 genomes] |
rs7526815 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7534679 | 0.86[ASN][1000 genomes] |
rs977019 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1829614 | chr1:160465291-160595000 | Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | nsv872491 | chr1:160470258-160580549 | Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
3 | nsv831703 | chr1:160496124-160643024 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
4 | esv1822379 | chr1:160545332-160831143 | Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:160555600-160575200 | Weak transcription | Primary T helper 17 cells PMA-I stimulated | -- |
2 | chr1:160558000-160575400 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |