Variant report
| Variant | rs73655894 |
|---|---|
| Chromosome Location | chr9:116505140-116505141 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:116502200-116505200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr9:116504400-116505600 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
| 3 | chr9:116504600-116505200 | Enhancers | HMEC | breast |
| 4 | chr9:116504800-116505200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 5 | chr9:116504800-116505400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 6 | chr9:116504800-116505400 | Enhancers | Spleen | Spleen |
| 7 | chr9:116504800-116505600 | Enhancers | H1 Cell Line | embryonic stem cell |
| 8 | chr9:116504800-116505600 | Enhancers | HUES6 Cell Line | embryonic stem cell |
| 9 | chr9:116505000-116505200 | Bivalent Enhancer | iPS-15b Cell Line | embryonic stem cell |
| 10 | chr9:116505000-116505200 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
| 11 | chr9:116505000-116505400 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
| 12 | chr9:116505000-116505400 | Bivalent Enhancer | NHEK | skin |
| 13 | chr9:116505000-116506400 | Enhancers | Fetal Heart | heart |
