Variant report
| Variant | rs73576058 |
|---|---|
| Chromosome Location | chr16:79929859-79929860 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr16:79908800-79931400 | Weak transcription | Right Atrium | heart |
| 2 | chr16:79927800-79930400 | Weak transcription | HepG2 | liver |
| 3 | chr16:79929000-79933400 | Enhancers | Liver | Liver |
| 4 | chr16:79929000-79934400 | Enhancers | Fetal Intestine Small | intestine |
| 5 | chr16:79929200-79934600 | Enhancers | Fetal Intestine Large | intestine |
| 6 | chr16:79929400-79930600 | Enhancers | Brain Germinal Matrix | brain |
| 7 | chr16:79929400-79930800 | Weak transcription | K562 | blood |
| 8 | chr16:79929400-79934000 | Weak transcription | Small Intestine | intestine |
| 9 | chr16:79929400-79934400 | Enhancers | Duodenum Mucosa | Duodenum |
| 10 | chr16:79929600-79930000 | Enhancers | Esophagus | oesophagus |
| 11 | chr16:79929600-79930400 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 12 | chr16:79929600-79931800 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
