Variant report
| Variant | rs12303870 |
|---|---|
| Chromosome Location | chr12:44405114-44405115 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44390800-44439200 | Weak transcription | Esophagus | oesophagus |
| 2 | chr12:44402000-44432200 | Weak transcription | Aorta | Aorta |
| 3 | chr12:44402800-44414600 | Weak transcription | HSMMtube | muscle |
| 4 | chr12:44403600-44415600 | Weak transcription | Fetal Intestine Large | intestine |
| 5 | chr12:44403800-44405200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 6 | chr12:44403800-44409400 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 7 | chr12:44404000-44422600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 8 | chr12:44404200-44414600 | Weak transcription | Fetal Intestine Small | intestine |
| 9 | chr12:44404200-44422800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 10 | chr12:44404400-44416400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
