Variant report
| Variant | rs1469786 |
|---|---|
| Chromosome Location | chr1:213461960-213461961 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:213440000-213469800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr1:213440800-213465800 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
| 3 | chr1:213458400-213466400 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
| 4 | chr1:213461400-213462000 | Enhancers | HepG2 | liver |
| 5 | chr1:213461600-213462400 | Enhancers | Gastric | stomach |
