Variant report
| Variant | rs17380788 |
|---|---|
| Chromosome Location | chr12:26342243-26342244 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:26338800-26348200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr12:26340000-26342600 | Enhancers | HSMMtube | muscle |
| 3 | chr12:26341000-26343000 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 4 | chr12:26341800-26348000 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
| 5 | chr12:26341800-26348000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 6 | chr12:26341800-26348000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 7 | chr12:26341800-26348000 | Weak transcription | A549 | lung |
| 8 | chr12:26341800-26348000 | Weak transcription | NH-A | brain |
| 9 | chr12:26341800-26348000 | Weak transcription | NHEK | skin |
| 10 | chr12:26341800-26348000 | Weak transcription | Osteobl | bone |
