Variant report
| Variant | rs72824072 |
|---|---|
| Chromosome Location | chr6:11979086-11979087 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:11973200-11980200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr6:11975800-11979200 | Enhancers | K562 | blood |
| 3 | chr6:11978200-11979600 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
| 4 | chr6:11978400-11979200 | Enhancers | Fetal Intestine Large | intestine |
| 5 | chr6:11978400-11979200 | Enhancers | HUVEC | blood vessel |
| 6 | chr6:11978400-11979400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 7 | chr6:11978600-11979200 | Enhancers | Primary T helper naive cells fromperipheralblood | blood |
| 8 | chr6:11978600-11979200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 9 | chr6:11978600-11979200 | Enhancers | Fetal Intestine Small | intestine |
| 10 | chr6:11978600-11979200 | Enhancers | NH-A | brain |
| 11 | chr6:11978600-11979400 | Enhancers | Primary hematopoietic stem cells | blood |
