Variant report
| Variant | rs12049416 |
|---|---|
| Chromosome Location | chr1:47872078-47872079 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:47847600-47872800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 2 | chr1:47868800-47873800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 3 | chr1:47869200-47872400 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr1:47871200-47872200 | Bivalent Enhancer | Fetal Lung | lung |
| 5 | chr1:47871600-47872200 | Enhancers | NHDF-Ad | bronchial |
| 6 | chr1:47871800-47872800 | Weak transcription | HSMM | muscle |
| 7 | chr1:47871800-47873200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 8 | chr1:47871800-47875000 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 9 | chr1:47871800-47875200 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 10 | chr1:47872000-47874800 | Weak transcription | Fetal Kidney | kidney |
