Variant report
| Variant | rs296648 |
|---|---|
| Chromosome Location | chr9:93829019-93829020 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:93824000-93833400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 2 | chr9:93824600-93833400 | Weak transcription | NHLF | lung |
| 3 | chr9:93824800-93833400 | Weak transcription | Spleen | Spleen |
| 4 | chr9:93826200-93833600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 5 | chr9:93826600-93833400 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
| 6 | chr9:93828000-93833400 | Weak transcription | Esophagus | oesophagus |
| 7 | chr9:93828200-93833200 | Weak transcription | HepG2 | liver |
| 8 | chr9:93828800-93836400 | Weak transcription | Right Ventricle | heart |
| 9 | chr9:93829000-93829200 | Bivalent Enhancer | Foreskin Melanocyte Primary Cells skin01 | Skin |
