Variant report
| Variant | rs67934834 |
|---|---|
| Chromosome Location | chr7:98899464-98899465 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:98873200-98905800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 2 | chr7:98874800-98906800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 3 | chr7:98890800-98905800 | Weak transcription | Pancreas | Pancrea |
| 4 | chr7:98893200-98906600 | Weak transcription | Fetal Intestine Small | intestine |
| 5 | chr7:98893800-98906000 | Weak transcription | HMEC | breast |
| 6 | chr7:98897200-98903200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 7 | chr7:98899200-98907800 | Weak transcription | Aorta | Aorta |
| 8 | chr7:98899400-98899600 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 9 | chr7:98899400-98901800 | Weak transcription | Gastric | stomach |
| 10 | chr7:98899400-98907000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 11 | chr7:98899400-98907200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
