Variant report
| Variant | rs28617180 |
|---|---|
| Chromosome Location | chr8:126503615-126503616 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:126498600-126509200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 2 | chr8:126498600-126509800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 3 | chr8:126502200-126509800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 4 | chr8:126502600-126504200 | Enhancers | Liver | Liver |
| 5 | chr8:126503000-126504000 | Flanking Active TSS | Primary neutrophils fromperipheralblood | blood |
| 6 | chr8:126503000-126504200 | Enhancers | Adipose Nuclei | Adipose |
| 7 | chr8:126503000-126504400 | Enhancers | Placenta | Placenta |
| 8 | chr8:126503200-126504200 | Enhancers | Primary B cells from cord blood | blood |
| 9 | chr8:126503400-126503800 | Flanking Active TSS | HepG2 | liver |
| 10 | chr8:126503600-126505000 | Weak transcription | Primary hematopoietic stem cells | blood |
