Variant report
| Variant | rs7793636 |
|---|---|
| Chromosome Location | chr7:121474862-121474863 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:121471400-121475600 | Enhancers | Fetal Brain Male | brain |
| 2 | chr7:121471800-121477000 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 3 | chr7:121472400-121475000 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 4 | chr7:121472800-121479000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 5 | chr7:121474600-121477000 | Weak transcription | Fetal Brain Female | brain |
| 6 | chr7:121474800-121476000 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
