Variant report
| Variant | rs12000926 |
|---|---|
| Chromosome Location | chr9:16189079-16189080 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:16179800-16192000 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 2 | chr9:16185000-16189200 | Weak transcription | Primary T cells from cord blood | blood |
| 3 | chr9:16185200-16193600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 4 | chr9:16185600-16192200 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
| 5 | chr9:16185600-16196400 | Weak transcription | Aorta | Aorta |
| 6 | chr9:16187800-16191400 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 7 | chr9:16189000-16190000 | ZNF genes & repeats | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
