Variant report
| Variant | rs11811483 |
|---|---|
| Chromosome Location | chr1:59073835-59073836 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:59060600-59082200 | Weak transcription | HUVEC | blood vessel |
| 2 | chr1:59061200-59074000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr1:59062600-59074600 | Weak transcription | NHEK | skin |
| 4 | chr1:59062800-59074800 | Weak transcription | HMEC | breast |
| 5 | chr1:59065200-59074800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 6 | chr1:59067400-59074200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr1:59071400-59077400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 8 | chr1:59072400-59074000 | Weak transcription | Stomach Mucosa | stomach |
| 9 | chr1:59072800-59082800 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 10 | chr1:59073200-59075000 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 11 | chr1:59073400-59074800 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
| 12 | chr1:59073400-59077800 | Weak transcription | Aorta | Aorta |
