Variant report
| Variant | rs7805584 |
|---|---|
| Chromosome Location | chr7:139995054-139995055 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:139975600-140002600 | Weak transcription | Right Atrium | heart |
| 2 | chr7:139977400-139995400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 3 | chr7:139986800-140007800 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr7:139993800-139995400 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 5 | chr7:139994600-139999800 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 6 | chr7:139994600-140004000 | Weak transcription | K562 | blood |
| 7 | chr7:139995000-140000200 | Weak transcription | HepG2 | liver |
