Variant report
| Variant | rs11182547 |
|---|---|
| Chromosome Location | chr12:44984256-44984257 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44940200-44999600 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
| 2 | chr12:44943400-44998600 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
| 3 | chr12:44966800-45000600 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
| 4 | chr12:44977200-44984400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 5 | chr12:44977400-44988600 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 6 | chr12:44977400-44995200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 7 | chr12:44977400-44998800 | Weak transcription | Primary T cells fromperipheralblood | blood |
| 8 | chr12:44983600-44984800 | Enhancers | HUES64 Cell Line | embryonic stem cell |
| 9 | chr12:44983800-44992000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 10 | chr12:44984200-44984600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
