Variant report
| Variant | rs35772088 |
|---|---|
| Chromosome Location | chr9:104049671-104049672 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:104038200-104054000 | Weak transcription | Fetal Brain Male | brain |
| 2 | chr9:104039200-104050000 | Weak transcription | HepG2 | liver |
| 3 | chr9:104041400-104053000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 4 | chr9:104043400-104053400 | Weak transcription | Brain Cingulate Gyrus | brain |
| 5 | chr9:104046000-104056400 | Weak transcription | Brain Anterior Caudate | brain |
| 6 | chr9:104046000-104061800 | Weak transcription | Brain Substantia Nigra | brain |
| 7 | chr9:104048600-104051600 | Strong transcription | Fetal Brain Female | brain |
| 8 | chr9:104048800-104071600 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 9 | chr9:104049600-104052600 | Strong transcription | Brain Hippocampus Middle | brain |
