Variant report
Variant | rs9694357 |
---|---|
Chromosome Location | chr8:49581503-49581504 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:49570000-49584000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr8:49573400-49586000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr8:49580200-49586600 | Enhancers | Fetal Lung | lung |
4 | chr8:49581000-49581600 | Enhancers | Monocytes-CD14+_RO01746 | blood |
5 | chr8:49581200-49581600 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
6 | chr8:49581200-49581600 | Enhancers | Primary monocytes fromperipheralblood | blood |
7 | chr8:49581200-49581600 | Enhancers | Fetal Heart | heart |
8 | chr8:49581200-49587800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
9 | chr8:49581400-49581800 | Enhancers | Fetal Stomach | stomach |