Variant report
| Variant | rs16848779 |
|---|---|
| Chromosome Location | chr3:138843228-138843229 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:138836200-138843400 | Enhancers | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 2 | chr3:138836600-138843400 | Enhancers | HSMM | muscle |
| 3 | chr3:138836600-138846800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 4 | chr3:138839400-138849200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 5 | chr3:138839800-138843400 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 6 | chr3:138839800-138843600 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 7 | chr3:138839800-138847200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 8 | chr3:138841600-138845800 | Weak transcription | Osteobl | bone |
| 9 | chr3:138841800-138849000 | Weak transcription | Pancreas | Pancrea |
| 10 | chr3:138842200-138845800 | Weak transcription | K562 | blood |
| 11 | chr3:138842800-138845600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 12 | chr3:138843000-138843600 | Enhancers | NHDF-Ad | bronchial |
| 13 | chr3:138843200-138843400 | Enhancers | Sigmoid Colon | Sigmoid Colon |
