Variant report
| Variant | rs74069736 |
|---|---|
| Chromosome Location | chr14:79809928-79809929 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:79792200-79825600 | Weak transcription | Aorta | Aorta |
| 2 | chr14:79798800-79811600 | Weak transcription | Colon Smooth Muscle | Colon |
| 3 | chr14:79808400-79810000 | Enhancers | H9 Cell Line | embryonic stem cell |
| 4 | chr14:79808400-79810800 | Enhancers | Placenta Amnion | Placenta Amnion |
| 5 | chr14:79808600-79810800 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 6 | chr14:79809000-79810000 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 7 | chr14:79809000-79810200 | Enhancers | Placenta | Placenta |
| 8 | chr14:79809000-79810400 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 9 | chr14:79809000-79810400 | Enhancers | NHEK | skin |
| 10 | chr14:79809800-79813000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
