Variant report
| Variant | rs55877668 |
|---|---|
| Chromosome Location | chr2:48346640-48346641 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:48340800-48347800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 2 | chr2:48342200-48348200 | Weak transcription | Primary hematopoietic stem cells | blood |
| 3 | chr2:48342200-48353000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 4 | chr2:48342400-48347000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 5 | chr2:48342400-48347400 | Weak transcription | K562 | blood |
| 6 | chr2:48342400-48347800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr2:48342600-48347200 | Weak transcription | Hela-S3 | cervix |
| 8 | chr2:48342600-48348000 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
| 9 | chr2:48344400-48347000 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 10 | chr2:48344600-48347000 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 11 | chr2:48345800-48349000 | Enhancers | HepG2 | liver |
| 12 | chr2:48346600-48347000 | Enhancers | Brain Hippocampus Middle | brain |
