Variant report
| Variant | rs56826756 |
|---|---|
| Chromosome Location | chr2:113696988-113696989 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:113694000-113699200 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 2 | chr2:113695800-113697600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 3 | chr2:113696000-113697400 | Enhancers | HMEC | breast |
| 4 | chr2:113696200-113697000 | Flanking Active TSS | Liver | Liver |
| 5 | chr2:113696400-113697200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 6 | chr2:113696400-113697600 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 7 | chr2:113696600-113697000 | Enhancers | NH-A | brain |
| 8 | chr2:113696600-113697000 | Enhancers | NHEK | skin |
| 9 | chr2:113696600-113697000 | Enhancers | Osteobl | bone |
| 10 | chr2:113696600-113697200 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 11 | chr2:113696600-113697400 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 12 | chr2:113696600-113697400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 13 | chr2:113696800-113697200 | Weak transcription | Gastric | stomach |
| 14 | chr2:113696800-113697400 | Bivalent Enhancer | HepG2 | liver |
