Variant report
| Variant | rs17103619 |
|---|---|
| Chromosome Location | chr5:145068001-145068002 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:145060800-145074600 | Weak transcription | Aorta | Aorta |
| 2 | chr5:145060800-145089600 | Weak transcription | Gastric | stomach |
| 3 | chr5:145061400-145076800 | Weak transcription | Pancreas | Pancrea |
| 4 | chr5:145062000-145069200 | Weak transcription | HepG2 | liver |
| 5 | chr5:145062400-145071800 | Weak transcription | Rectal Smooth Muscle | rectum |
| 6 | chr5:145066600-145084200 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 7 | chr5:145067600-145070600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 8 | chr5:145067800-145068400 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 9 | chr5:145068000-145070400 | Enhancers | Brain Substantia Nigra | brain |
