Variant report
| Variant | rs536427790 |
|---|---|
| Chromosome Location | chr2:58958812-58958813 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:58948400-58960000 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 2 | chr2:58954600-58963200 | Enhancers | Primary hematopoietic stem cells | blood |
| 3 | chr2:58955000-58964400 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
| 4 | chr2:58958000-58959000 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 5 | chr2:58958000-58959200 | Flanking Active TSS | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 6 | chr2:58958600-58959000 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 7 | chr2:58958600-58959000 | Enhancers | HUVEC | blood vessel |
| 8 | chr2:58958600-58959800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
| 9 | chr2:58958800-58959000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
| 10 | chr2:58958800-58959000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 11 | chr2:58958800-58959000 | Flanking Active TSS | K562 | blood |
| 12 | chr2:58958800-58959800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 13 | chr2:58958800-58960000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 14 | chr2:58958800-58961400 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
