Variant report
| Variant | rs73388513 |
|---|---|
| Chromosome Location | chr12:106676833-106676834 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:106666200-106680800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 2 | chr12:106674000-106677000 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 3 | chr12:106674000-106677200 | Enhancers | Fetal Heart | heart |
| 4 | chr12:106676000-106677200 | Enhancers | Liver | Liver |
| 5 | chr12:106676200-106678200 | Weak transcription | NHEK | skin |
| 6 | chr12:106676200-106679200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 7 | chr12:106676400-106677200 | Enhancers | Fetal Intestine Large | intestine |
| 8 | chr12:106676400-106677200 | Enhancers | Fetal Intestine Small | intestine |
| 9 | chr12:106676600-106677000 | Enhancers | Rectal Mucosa Donor 31 | rectum |
| 10 | chr12:106676600-106681000 | Weak transcription | Stomach Mucosa | stomach |
| 11 | chr12:106676800-106677000 | Enhancers | Colonic Mucosa | Colon |
| 12 | chr12:106676800-106677200 | Flanking Active TSS | HepG2 | liver |
