Variant report
Variant | rs765388 |
---|---|
Chromosome Location | chr9:93831759-93831760 |
allele | A/G |
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 | chr9:93829800-93832600 | Enhancers | Primary neutrophils fromperipheralblood | blood |
10 | chr9:93830200-93833200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
11 | chr9:93831000-93833200 | Weak transcription | Fetal Intestine Large | intestine |
12 | chr9:93831600-93832000 | ZNF genes & repeats | Fetal Intestine Small | intestine |