Variant report
| Variant | rs1794624 |
|---|---|
| Chromosome Location | chr6:36535346-36535347 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:36525800-36540200 | Weak transcription | Placenta | Placenta |
| 2 | chr6:36534000-36535600 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 3 | chr6:36534600-36535800 | Flanking Active TSS | HepG2 | liver |
| 4 | chr6:36534800-36538000 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 5 | chr6:36535000-36535600 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
| 6 | chr6:36535000-36535600 | Active TSS | A549 | lung |
| 7 | chr6:36535000-36546400 | Weak transcription | Fetal Intestine Large | intestine |
| 8 | chr6:36535000-36546800 | Weak transcription | Primary B cells from cord blood | blood |
| 9 | chr6:36535200-36537800 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 10 | chr6:36535200-36551200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
