Variant report
Variant | rs191902 |
---|---|
Chromosome Location | chr6:33489431-33489432 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs1794687 | 0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs210177 | 0.84[EUR][1000 genomes] |
rs210178 | 0.85[EUR][1000 genomes] |
rs210180 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs210182 | 0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs210183 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs210184 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs210185 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs210186 | 0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs210187 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs210192 | 0.85[EUR][1000 genomes] |
rs210196 | 0.86[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs210197 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs367408 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs367897 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs368429 | 0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs368716 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs371155 | 0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs372469 | 0.84[EUR][1000 genomes] |
rs372846 | 0.84[EUR][1000 genomes] |
rs380163 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs383936 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs386879 | 0.87[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs3916269 | 0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs396516 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs404778 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs405126 | 0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs447418 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs449242 | 0.89[EUR][1000 genomes] |
rs73404347 | 0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9461874 | 0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9469481 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9469483 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830637 | chr6:33329365-33510704 | Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 62 gene(s) | inside rSNPs | diseases |
2 | nsv602832 | chr6:33382241-33520221 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 41 gene(s) | inside rSNPs | diseases |
3 | nsv524010 | chr6:33468151-33505981 | Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:33481400-33491200 | Weak transcription | Right Atrium | heart |
2 | chr6:33489200-33490000 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |