Variant report
| Variant | rs55788229 |
|---|---|
| Chromosome Location | chr2:48514639-48514640 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:48506000-48539000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 2 | chr2:48513800-48514800 | ZNF genes & repeats | Primary hematopoietic stem cells short term culture | blood |
| 3 | chr2:48514000-48516800 | ZNF genes & repeats | Primary B cells from peripheral blood | blood |
| 4 | chr2:48514000-48519400 | Weak transcription | Primary T cells from cord blood | blood |
| 5 | chr2:48514200-48517600 | Weak transcription | K562 | blood |
| 6 | chr2:48514400-48515600 | Enhancers | Primary hematopoietic stem cells | blood |
| 7 | chr2:48514400-48515800 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 8 | chr2:48514600-48515400 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
| 9 | chr2:48514600-48515800 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 10 | chr2:48514600-48516200 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
