Variant report
| Variant | rs10876844 |
|---|---|
| Chromosome Location | chr12:56050706-56050707 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:56045800-56050800 | Weak transcription | HepG2 | liver |
| 2 | chr12:56049000-56051400 | Weak transcription | Lung | lung |
| 3 | chr12:56049000-56052600 | Weak transcription | HSMM | muscle |
| 4 | chr12:56049800-56054200 | Enhancers | Fetal Intestine Small | intestine |
| 5 | chr12:56050000-56053600 | Enhancers | Fetal Intestine Large | intestine |
| 6 | chr12:56050200-56051400 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 7 | chr12:56050200-56052200 | Weak transcription | Fetal Heart | heart |
| 8 | chr12:56050200-56052800 | Enhancers | Duodenum Mucosa | Duodenum |
| 9 | chr12:56050400-56052200 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
| 10 | chr12:56050600-56050800 | Enhancers | Monocytes-CD14+_RO01746 | blood |
