Variant report
| Variant | rs6939552 |
|---|---|
| Chromosome Location | chr6:110374640-110374641 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:110373000-110375400 | Enhancers | Placenta | Placenta |
| 2 | chr6:110373800-110374800 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 3 | chr6:110374200-110375000 | Enhancers | Fetal Muscle Trunk | muscle |
| 4 | chr6:110374400-110375000 | Enhancers | Brain Cingulate Gyrus | brain |
| 5 | chr6:110374400-110375000 | Enhancers | Ovary | ovary |
| 6 | chr6:110374600-110374800 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
| 7 | chr6:110374600-110375000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 8 | chr6:110374600-110375000 | Enhancers | Brain Angular Gyrus | brain |
| 9 | chr6:110374600-110375000 | Active TSS | Brain Hippocampus Middle | brain |
| 10 | chr6:110374600-110375000 | Enhancers | Brain Substantia Nigra | brain |
