Variant report
| Variant | rs59275453 |
|---|---|
| Chromosome Location | chr11:16146989-16146990 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:16138800-16147600 | Weak transcription | Fetal Intestine Small | intestine |
| 2 | chr11:16140200-16148000 | Weak transcription | Psoas Muscle | Psoas |
| 3 | chr11:16141200-16147400 | Weak transcription | Brain Germinal Matrix | brain |
| 4 | chr11:16141200-16147800 | Weak transcription | Fetal Heart | heart |
| 5 | chr11:16141400-16147600 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
| 6 | chr11:16143800-16147600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 7 | chr11:16144000-16148000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 8 | chr11:16144600-16147000 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 9 | chr11:16145800-16149200 | Enhancers | HepG2 | liver |
| 10 | chr11:16146400-16149400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
