Variant report
| Variant | rs17106793 |
|---|---|
| Chromosome Location | chr14:69657199-69657200 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:69650800-69657600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 2 | chr14:69651200-69657200 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 3 | chr14:69651200-69657400 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
| 4 | chr14:69651200-69657800 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 5 | chr14:69651600-69657400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 6 | chr14:69656000-69657800 | Weak transcription | Right Atrium | heart |
| 7 | chr14:69656800-69657600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
| 8 | chr14:69656800-69658000 | Weak transcription | Gastric | stomach |
| 9 | chr14:69657000-69657400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
| 10 | chr14:69657000-69657400 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 11 | chr14:69657000-69657600 | Enhancers | HUES64 Cell Line | embryonic stem cell |
| 12 | chr14:69657000-69657600 | Bivalent Enhancer | Dnd41 | blood |
