Variant report
| Variant | rs11182371 |
|---|---|
| Chromosome Location | chr12:44394939-44394940 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44361400-44401400 | Weak transcription | Aorta | Aorta |
| 2 | chr12:44383200-44402400 | Weak transcription | HSMMtube | muscle |
| 3 | chr12:44384400-44399600 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr12:44387400-44399200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 5 | chr12:44387600-44399400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 6 | chr12:44390800-44439200 | Weak transcription | Esophagus | oesophagus |
| 7 | chr12:44394600-44400000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 8 | chr12:44394600-44403200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 9 | chr12:44394800-44399000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 10 | chr12:44394800-44401800 | Weak transcription | HMEC | breast |
