Variant report
| Variant | rs373042382 |
|---|---|
| Chromosome Location | chr8:126417169-126417170 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:126404400-126424400 | Weak transcription | Spleen | Spleen |
| 2 | chr8:126414000-126422800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 3 | chr8:126414400-126417200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 4 | chr8:126416000-126417200 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 5 | chr8:126416800-126417600 | Enhancers | Lung | lung |
| 6 | chr8:126417000-126417200 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 7 | chr8:126417000-126417600 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 8 | chr8:126417000-126417800 | Enhancers | HUES6 Cell Line | embryonic stem cell |
| 9 | chr8:126417000-126418000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 10 | chr8:126417000-126418200 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 11 | chr8:126417000-126418200 | Enhancers | HepG2 | liver |
| 12 | chr8:126417000-126418200 | Enhancers | HUVEC | blood vessel |
