Variant report
| Variant | rs73828092 |
|---|---|
| Chromosome Location | chr4:79594780-79594781 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr4:79586800-79595400 | Enhancers | Primary B cells from peripheral blood | blood |
| 2 | chr4:79589400-79595400 | Enhancers | Primary B cells from cord blood | blood |
| 3 | chr4:79590000-79595200 | Weak transcription | NHDF-Ad | bronchial |
| 4 | chr4:79591200-79594800 | Enhancers | Fetal Intestine Large | intestine |
| 5 | chr4:79593800-79595800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 6 | chr4:79594000-79598800 | Weak transcription | HepG2 | liver |
| 7 | chr4:79594400-79597800 | Weak transcription | K562 | blood |
| 8 | chr4:79594600-79598400 | Weak transcription | Fetal Intestine Small | intestine |
