Variant report
| Variant | rs7021753 |
|---|---|
| Chromosome Location | chr9:85195750-85195751 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:85195200-85196600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 2 | chr9:85195200-85196600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 3 | chr9:85195200-85198200 | Enhancers | Fetal Intestine Small | intestine |
| 4 | chr9:85195200-85205000 | Enhancers | Fetal Intestine Large | intestine |
| 5 | chr9:85195400-85195800 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
| 6 | chr9:85195400-85197000 | Weak transcription | Pancreas | Pancrea |
| 7 | chr9:85195600-85195800 | Enhancers | Stomach Mucosa | stomach |
| 8 | chr9:85195600-85200000 | Enhancers | Liver | Liver |
| 9 | chr9:85195600-85205200 | Enhancers | HepG2 | liver |
