Variant report
| Variant | rs73687925 |
|---|---|
| Chromosome Location | chr7:41185527-41185528 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:41174400-41187800 | Weak transcription | NHLF | lung |
| 2 | chr7:41175800-41185600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 3 | chr7:41183600-41187200 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 4 | chr7:41183800-41186600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr7:41184000-41186800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 6 | chr7:41184000-41186800 | Weak transcription | Osteobl | bone |
| 7 | chr7:41184800-41185800 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 8 | chr7:41185200-41185600 | Enhancers | H9 Cell Line | embryonic stem cell |
| 9 | chr7:41185200-41185800 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
| 10 | chr7:41185200-41186200 | Enhancers | Fetal Stomach | stomach |
| 11 | chr7:41185200-41187800 | Enhancers | NHEK | skin |
| 12 | chr7:41185200-41189600 | Enhancers | HMEC | breast |
| 13 | chr7:41185400-41187600 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
