Variant report
| Variant | rs59961542 |
|---|---|
| Chromosome Location | chr2:31234594-31234595 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:31232600-31235400 | Weak transcription | Fetal Lung | lung |
| 2 | chr2:31232600-31251000 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 3 | chr2:31232800-31235200 | Weak transcription | Fetal Kidney | kidney |
| 4 | chr2:31233400-31235200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 5 | chr2:31233800-31235400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 6 | chr2:31234400-31234800 | Bivalent Enhancer | Fetal Adrenal Gland | Adrenal Gland |
| 7 | chr2:31234400-31235200 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 8 | chr2:31234400-31236000 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 9 | chr2:31234400-31236000 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 10 | chr2:31234400-31236400 | Enhancers | NHEK | skin |
