Variant report
| Variant | rs55996795 |
|---|---|
| Chromosome Location | chr12:44369706-44369707 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44343600-44376800 | Weak transcription | Pancreas | Pancrea |
| 2 | chr12:44361400-44401400 | Weak transcription | Aorta | Aorta |
| 3 | chr12:44363800-44382400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 4 | chr12:44364600-44370000 | Weak transcription | HMEC | breast |
| 5 | chr12:44364600-44393200 | Weak transcription | Small Intestine | intestine |
| 6 | chr12:44364800-44377000 | Weak transcription | Left Ventricle | heart |
| 7 | chr12:44366000-44375600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 8 | chr12:44366200-44373400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 9 | chr12:44368800-44370800 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
| 10 | chr12:44368800-44371200 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 11 | chr12:44369600-44369800 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 12 | chr12:44369600-44370200 | Enhancers | NHEK | skin |
