Variant report
| Variant | rs16948612 |
|---|---|
| Chromosome Location | chr18:28525731-28525732 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr18:28524600-28526200 | Enhancers | Fetal Brain Male | brain |
| 2 | chr18:28524600-28526800 | Enhancers | Brain Germinal Matrix | brain |
| 3 | chr18:28524800-28526000 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
| 4 | chr18:28524800-28526800 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 5 | chr18:28524800-28527000 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
| 6 | chr18:28525000-28526000 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 7 | chr18:28525400-28526200 | Weak transcription | Fetal Brain Female | brain |
