Variant report
| Variant | rs9991565 |
|---|---|
| Chromosome Location | chr4:166374880-166374881 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr4:166361800-166375200 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 2 | chr4:166362200-166381600 | Weak transcription | Fetal Stomach | stomach |
| 3 | chr4:166362400-166381600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 4 | chr4:166362400-166382400 | Weak transcription | Aorta | Aorta |
| 5 | chr4:166362400-166384600 | Weak transcription | Brain Cingulate Gyrus | brain |
| 6 | chr4:166362600-166379000 | Weak transcription | Fetal Brain Female | brain |
| 7 | chr4:166362800-166379200 | Weak transcription | Brain Anterior Caudate | brain |
| 8 | chr4:166370800-166375000 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 9 | chr4:166372400-166379000 | Weak transcription | Fetal Brain Male | brain |
| 10 | chr4:166374800-166376000 | Enhancers | HepG2 | liver |
