Variant report
Variant | rs11176921 |
---|---|
Chromosome Location | chr12:40898064-40898065 |
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] |
---|---|
rs11176706 | 0.88[ASN][1000 genomes] |
rs11176796 | 0.88[ASN][1000 genomes] |
rs11176808 | 0.88[ASN][1000 genomes] |
rs11176811 | 0.88[ASN][1000 genomes] |
rs11176815 | 0.88[ASN][1000 genomes] |
rs11176824 | 0.88[ASN][1000 genomes] |
rs11176825 | 0.88[ASN][1000 genomes] |
rs11176826 | 0.88[ASN][1000 genomes] |
rs11176844 | 0.83[ASN][1000 genomes] |
rs11176922 | 0.96[ASN][1000 genomes] |
rs11564168 | 0.85[ASN][1000 genomes] |
rs12368100 | 0.98[ASN][1000 genomes] |
rs12822472 | 0.96[ASN][1000 genomes] |
rs17492159 | 1.00[CHB][hapmap] |
rs17520991 | 1.00[CHB][hapmap] |
rs17531348 | 0.88[ASN][1000 genomes] |
rs17597194 | 0.83[ASN][1000 genomes] |
rs17597222 | 0.88[ASN][1000 genomes] |
rs28365238 | 1.00[CHB][hapmap] |
rs74076586 | 0.88[ASN][1000 genomes] |
rs74076588 | 0.85[ASN][1000 genomes] |
rs74076590 | 0.85[ASN][1000 genomes] |
rs74076593 | 0.81[ASN][1000 genomes] |
rs74079003 | 0.92[ASN][1000 genomes] |
rs74079018 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv899033 | chr12:40758652-41122288 | Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:40894800-40908600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |