Variant report
| Variant | rs10165927 |
|---|---|
| Chromosome Location | chr2:160925835-160925836 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:160921000-160930200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 2 | chr2:160921600-160926000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr2:160922600-160928000 | Weak transcription | Fetal Intestine Large | intestine |
