Variant report
| Variant | rs1545784 |
|---|---|
| Chromosome Location | chr12:26283469-26283470 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:26280000-26287800 | Weak transcription | Aorta | Aorta |
| 2 | chr12:26280400-26286800 | Weak transcription | Brain Substantia Nigra | brain |
| 3 | chr12:26280600-26287800 | Weak transcription | Brain Hippocampus Middle | brain |
| 4 | chr12:26280600-26290200 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
| 5 | chr12:26281200-26286600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 6 | chr12:26281600-26286600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr12:26281600-26286600 | Weak transcription | HMEC | breast |
| 8 | chr12:26282800-26286000 | Enhancers | Primary B cells from peripheral blood | blood |
| 9 | chr12:26283200-26283600 | Bivalent Enhancer | Monocytes-CD14+_RO01746 | blood |
| 10 | chr12:26283400-26284600 | Enhancers | Primary B cells from cord blood | blood |
