Variant report
Variant | rs17270896 |
---|---|
Chromosome Location | chr2:182255121-182255122 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11690881 | 0.98[ASN][1000 genomes] |
rs17198633 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs17198689 | 0.91[ASN][1000 genomes] |
rs17198696 | 0.91[ASN][1000 genomes] |
rs17198703 | 0.91[ASN][1000 genomes] |
rs17198710 | 0.91[ASN][1000 genomes] |
rs17198717 | 0.96[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs17270868 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17270882 | 0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs17270889 | 0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs17270903 | 0.82[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs17365432 | 0.88[CHB][hapmap] |
rs35262123 | 0.98[ASN][1000 genomes] |
rs62180253 | 0.83[ASN][1000 genomes] |
rs62180258 | 0.82[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs62182269 | 0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs62189833 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs62189855 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62189857 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62189858 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62189859 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6726597 | 0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6726903 | 0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9646799 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1005870 | chr2:181968637-182921439 | Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
2 | nsv536063 | chr2:181968637-182921439 | Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
3 | nsv1002647 | chr2:182078521-182392273 | Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv536064 | chr2:182078521-182392273 | Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
5 | nsv834476 | chr2:182179249-182360259 | Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:182238000-182258200 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
2 | chr2:182240000-182257400 | Weak transcription | Primary T helper memory cells from peripheral blood 1 | blood |
3 | chr2:182241600-182258200 | Weak transcription | Fetal Thymus | thymus |