Variant report
| Variant | rs73876908 |
|---|---|
| Chromosome Location | chr3:155386898-155386899 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:155383400-155387000 | Enhancers | HepG2 | liver |
| 2 | chr3:155383400-155390200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 3 | chr3:155383400-155393800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 4 | chr3:155383400-155394000 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 5 | chr3:155383400-155395800 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 6 | chr3:155383600-155394000 | Weak transcription | Pancreas | Pancrea |
| 7 | chr3:155385200-155394000 | Weak transcription | Duodenum Mucosa | Duodenum |
| 8 | chr3:155385400-155390000 | Weak transcription | Fetal Intestine Large | intestine |
| 9 | chr3:155386200-155390000 | Weak transcription | Fetal Intestine Small | intestine |
