Variant report
| Variant | rs4501019 |
|---|---|
| Chromosome Location | chr20:22447016-22447017 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr20:22439400-22448400 | Enhancers | Stomach Mucosa | stomach |
| 2 | chr20:22444400-22448000 | Enhancers | A549 | lung |
| 3 | chr20:22445000-22448200 | Enhancers | Pancreas | Pancrea |
| 4 | chr20:22446200-22447400 | Enhancers | K562 | blood |
| 5 | chr20:22446200-22448200 | Enhancers | Liver | Liver |
| 6 | chr20:22446400-22451600 | Weak transcription | Gastric | stomach |
| 7 | chr20:22446800-22448200 | Flanking Bivalent TSS/Enh | HepG2 | liver |
| 8 | chr20:22447000-22448200 | Bivalent Enhancer | Fetal Intestine Large | intestine |
| 9 | chr20:22447000-22450800 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
