Variant report
| Variant | rs11050936 |
|---|---|
| Chromosome Location | chr12:30667304-30667305 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:30662000-30668800 | Weak transcription | Pancreas | Pancrea |
| 2 | chr12:30664400-30671400 | Weak transcription | HepG2 | liver |
| 3 | chr12:30665400-30667600 | Weak transcription | Fetal Brain Male | brain |
| 4 | chr12:30666200-30667800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 5 | chr12:30666200-30668800 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 6 | chr12:30666600-30668200 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
| 7 | chr12:30666600-30668600 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
| 8 | chr12:30666800-30667600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
| 9 | chr12:30667000-30667400 | Enhancers | Fetal Stomach | stomach |
| 10 | chr12:30667000-30668200 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
| 11 | chr12:30667200-30668000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
