Variant report
Variant | rs11511171 |
---|---|
Chromosome Location | chr10:23171862-23171863 |
allele | A/C |
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] |
---|---|
rs10128359 | 1.00[ASN][1000 genomes] |
rs11013245 | 1.00[ASN][1000 genomes] |
rs11013246 | 1.00[ASN][1000 genomes] |
rs11013247 | 1.00[ASN][1000 genomes] |
rs11013248 | 1.00[ASN][1000 genomes] |
rs11013250 | 1.00[ASN][1000 genomes] |
rs11013251 | 1.00[ASN][1000 genomes] |
rs11013252 | 1.00[ASN][1000 genomes] |
rs11013253 | 1.00[ASN][1000 genomes] |
rs11013255 | 1.00[ASN][1000 genomes] |
rs11013261 | 1.00[ASN][1000 genomes] |
rs11013262 | 1.00[ASN][1000 genomes] |
rs11013263 | 1.00[ASN][1000 genomes] |
rs11013264 | 1.00[ASN][1000 genomes] |
rs12243596 | 1.00[ASN][1000 genomes] |
rs12246105 | 1.00[ASN][1000 genomes] |
rs12249666 | 1.00[ASN][1000 genomes] |
rs12257453 | 1.00[ASN][1000 genomes] |
rs12257887 | 1.00[ASN][1000 genomes] |
rs12259839 | 1.00[ASN][1000 genomes] |
rs12261088 | 1.00[ASN][1000 genomes] |
rs12261456 | 1.00[ASN][1000 genomes] |
rs12264038 | 1.00[ASN][1000 genomes] |
rs12269590 | 1.00[ASN][1000 genomes] |
rs12763092 | 1.00[ASN][1000 genomes] |
rs12763296 | 1.00[ASN][1000 genomes] |
rs12773226 | 1.00[ASN][1000 genomes] |
rs12773873 | 1.00[ASN][1000 genomes] |
rs12784450 | 1.00[ASN][1000 genomes] |
rs34243414 | 1.00[ASN][1000 genomes] |
rs34853435 | 1.00[ASN][1000 genomes] |
rs34934641 | 1.00[ASN][1000 genomes] |
rs35627133 | 1.00[ASN][1000 genomes] |
rs35840125 | 1.00[ASN][1000 genomes] |
rs36053598 | 1.00[ASN][1000 genomes] |
rs59709734 | 1.00[ASN][1000 genomes] |
rs66468760 | 1.00[ASN][1000 genomes] |
rs66482823 | 1.00[ASN][1000 genomes] |
rs66815792 | 1.00[ASN][1000 genomes] |
rs67480460 | 1.00[ASN][1000 genomes] |
rs67750769 | 1.00[ASN][1000 genomes] |
rs67798485 | 1.00[ASN][1000 genomes] |
rs7089828 | 1.00[ASN][1000 genomes] |
rs72800633 | 1.00[ASN][1000 genomes] |
rs72812467 | 1.00[ASN][1000 genomes] |
rs7358041 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2764013 | chr10:23087298-23239345 | Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | nsv894966 | chr10:23090535-23202522 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:23170000-23174600 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr10:23170000-23174600 | Weak transcription | Pancreas | Pancrea |
3 | chr10:23170200-23174600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |