Variant report
| Variant | rs12993216 |
|---|---|
| Chromosome Location | chr10:60171373-60171374 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:60146000-60174200 | Weak transcription | Aorta | Aorta |
| 2 | chr10:60149800-60174600 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 3 | chr10:60155400-60174200 | Weak transcription | NHLF | lung |
| 4 | chr10:60156200-60174600 | Weak transcription | Fetal Muscle Leg | muscle |
| 5 | chr10:60156400-60172200 | Weak transcription | HepG2 | liver |
| 6 | chr10:60157800-60171800 | Weak transcription | HSMM | muscle |
| 7 | chr10:60160600-60173600 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 8 | chr10:60161200-60172000 | Weak transcription | Muscle Satellite Cultured Cells | -- |
| 9 | chr10:60168800-60172400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 10 | chr10:60170200-60172400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 11 | chr10:60171200-60171400 | Enhancers | Primary mononuclear cells fromperipheralblood | Blood |
