Variant report
| Variant | rs16849091 |
|---|---|
| Chromosome Location | chr2:213559282-213559283 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:213558000-213563200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 2 | chr2:213558800-213560400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 3 | chr2:213559200-213559600 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
