Variant report
| Variant | rs12088588 |
|---|---|
| Chromosome Location | chr1:175001850-175001851 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:174993200-175004800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr1:174993200-175013800 | Weak transcription | Spleen | Spleen |
| 3 | chr1:174998800-175003800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 4 | chr1:174999000-175004000 | Weak transcription | HMEC | breast |
| 5 | chr1:174999000-175005000 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
| 6 | chr1:174999400-175002200 | Weak transcription | Fetal Brain Male | brain |
| 7 | chr1:174999400-175003200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 8 | chr1:174999400-175005000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 9 | chr1:174999400-175006400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 10 | chr1:175001800-175003800 | Enhancers | Pancreatic Islets | Pancreatic Islet |
