Variant report
| Variant | rs2700056 |
|---|---|
| Chromosome Location | chr12:67951901-67951902 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:67949800-67953400 | Weak transcription | Fetal Thymus | thymus |
| 2 | chr12:67950200-67960000 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
| 3 | chr12:67951600-67952200 | Enhancers | Stomach Mucosa | stomach |
| 4 | chr12:67951600-67952400 | Enhancers | Fetal Intestine Small | intestine |
| 5 | chr12:67951800-67952800 | Enhancers | Duodenum Mucosa | Duodenum |
