Variant report
| Variant | rs644634 |
|---|---|
| Chromosome Location | chr6:36543698-36543699 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:36535000-36546400 | Weak transcription | Fetal Intestine Large | intestine |
| 2 | chr6:36535000-36546800 | Weak transcription | Primary B cells from cord blood | blood |
| 3 | chr6:36535200-36551200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 4 | chr6:36540000-36547800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 5 | chr6:36541000-36544600 | Weak transcription | Fetal Intestine Small | intestine |
| 6 | chr6:36541400-36544400 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
| 7 | chr6:36541400-36544400 | Weak transcription | A549 | lung |
| 8 | chr6:36541400-36544400 | Weak transcription | Hela-S3 | cervix |
| 9 | chr6:36542000-36544000 | Weak transcription | Placenta | Placenta |
| 10 | chr6:36542400-36544000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 11 | chr6:36542800-36545200 | Enhancers | HepG2 | liver |
