Variant report
| Variant | rs11051496 |
|---|---|
| Chromosome Location | chr12:31785056-31785057 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:31783400-31789800 | Weak transcription | Placenta | Placenta |
| 2 | chr12:31783400-31803000 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
| 3 | chr12:31783400-31803000 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr12:31783600-31792600 | Weak transcription | Pancreas | Pancrea |
| 5 | chr12:31783800-31785400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 6 | chr12:31783800-31789600 | Weak transcription | Adipose Nuclei | Adipose |
| 7 | chr12:31784000-31786200 | Enhancers | Primary B cells from peripheral blood | blood |
| 8 | chr12:31784200-31786000 | Enhancers | Primary B cells from cord blood | blood |
| 9 | chr12:31784400-31785600 | Enhancers | GM12878-XiMat | blood |
| 10 | chr12:31784600-31785400 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 11 | chr12:31784600-31794000 | Weak transcription | Ovary | ovary |
| 12 | chr12:31784800-31785600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 13 | chr12:31784800-31785600 | Enhancers | K562 | blood |
| 14 | chr12:31784800-31788200 | Weak transcription | Fetal Heart | heart |
| 15 | chr12:31785000-31785800 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
