Variant report
Variant | rs9940653 |
---|---|
Chromosome Location | chr16:80076378-80076379 |
allele | A/C |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:80072800-80085200 | Weak transcription | Esophagus | oesophagus |
2 | chr16:80073200-80078000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr16:80074200-80076800 | Enhancers | Placenta Amnion | Placenta Amnion |
4 | chr16:80074400-80076400 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
5 | chr16:80075000-80079600 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr16:80075800-80077400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
7 | chr16:80076000-80078200 | Enhancers | Fetal Stomach | stomach |
8 | chr16:80076000-80079600 | Weak transcription | Fetal Intestine Large | intestine |